NM_007294.4(BRCA1):c.4015G>A (p.Glu1339Lys) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 12, 2014
- Review status:
- 1 star out of maximum of 4 starscriteria provided, single submitter
- Somatic classification
of clinical impact: - None
- Review status:
- (0/4) 0 stars out of maximum of 4 starsno assertion criteria provided
- Somatic classification
of oncogenicity: - None
- Review status:
- (0/4) 0 stars out of maximum of 4 starsno assertion criteria provided
- Record status:
- current
- Accession:
- RCV000159985.2
Allele description [Variation Report for NM_007294.4(BRCA1):c.4015G>A (p.Glu1339Lys)]
NM_007294.4(BRCA1):c.4015G>A (p.Glu1339Lys)
- Genes:
- BRCA1:BRCA1 DNA repair associated [Gene - OMIM - HGNC]
LOC126862571:BRD4-independent group 4 enhancer GRCh37_chr17:41243136-41244335 [Gene] - Variant type:
- single nucleotide variant
- Cytogenetic location:
- 17q21.31
- Genomic location:
- Preferred name:
- NM_007294.4(BRCA1):c.4015G>A (p.Glu1339Lys)
- Other names:
- p.E1339K:GAA>AAA
- HGVS:
- NC_000017.11:g.43091516C>T
- NG_005905.2:g.126468G>A
- NG_087068.1:g.498C>T
- NM_001407571.1:c.3802G>A
- NM_001407581.1:c.4015G>A
- NM_001407582.1:c.4015G>A
- NM_001407583.1:c.4015G>A
- NM_001407585.1:c.4015G>A
- NM_001407587.1:c.4012G>A
- NM_001407590.1:c.4012G>A
- NM_001407591.1:c.4012G>A
- NM_001407593.1:c.4015G>A
- NM_001407594.1:c.4015G>A
- NM_001407596.1:c.4015G>A
- NM_001407597.1:c.4015G>A
- NM_001407598.1:c.4015G>A
- NM_001407602.1:c.4015G>A
- NM_001407603.1:c.4015G>A
- NM_001407605.1:c.4015G>A
- NM_001407610.1:c.4012G>A
- NM_001407611.1:c.4012G>A
- NM_001407612.1:c.4012G>A
- NM_001407613.1:c.4012G>A
- NM_001407614.1:c.4012G>A
- NM_001407615.1:c.4012G>A
- NM_001407616.1:c.4015G>A
- NM_001407617.1:c.4015G>A
- NM_001407618.1:c.4015G>A
- NM_001407619.1:c.4015G>A
- NM_001407620.1:c.4015G>A
- NM_001407621.1:c.4015G>A
- NM_001407622.1:c.4015G>A
- NM_001407623.1:c.4015G>A
- NM_001407624.1:c.4015G>A
- NM_001407625.1:c.4015G>A
- NM_001407626.1:c.4015G>A
- NM_001407627.1:c.4012G>A
- NM_001407628.1:c.4012G>A
- NM_001407629.1:c.4012G>A
- NM_001407630.1:c.4012G>A
- NM_001407631.1:c.4012G>A
- NM_001407632.1:c.4012G>A
- NM_001407633.1:c.4012G>A
- NM_001407634.1:c.4012G>A
- NM_001407635.1:c.4012G>A
- NM_001407636.1:c.4012G>A
- NM_001407637.1:c.4012G>A
- NM_001407638.1:c.4012G>A
- NM_001407639.1:c.4015G>A
- NM_001407640.1:c.4015G>A
- NM_001407641.1:c.4015G>A
- NM_001407642.1:c.4015G>A
- NM_001407644.1:c.4012G>A
- NM_001407645.1:c.4012G>A
- NM_001407646.1:c.4006G>A
- NM_001407647.1:c.4006G>A
- NM_001407648.1:c.3892G>A
- NM_001407649.1:c.3889G>A
- NM_001407652.1:c.4015G>A
- NM_001407653.1:c.3937G>A
- NM_001407654.1:c.3937G>A
- NM_001407655.1:c.3937G>A
- NM_001407656.1:c.3937G>A
- NM_001407657.1:c.3937G>A
- NM_001407658.1:c.3937G>A
- NM_001407659.1:c.3934G>A
- NM_001407660.1:c.3934G>A
- NM_001407661.1:c.3934G>A
- NM_001407662.1:c.3934G>A
- NM_001407663.1:c.3937G>A
- NM_001407664.1:c.3892G>A
- NM_001407665.1:c.3892G>A
- NM_001407666.1:c.3892G>A
- NM_001407667.1:c.3892G>A
- NM_001407668.1:c.3892G>A
- NM_001407669.1:c.3892G>A
- NM_001407670.1:c.3889G>A
- NM_001407671.1:c.3889G>A
- NM_001407672.1:c.3889G>A
- NM_001407673.1:c.3889G>A
- NM_001407674.1:c.3892G>A
- NM_001407675.1:c.3892G>A
- NM_001407676.1:c.3892G>A
- NM_001407677.1:c.3892G>A
- NM_001407678.1:c.3892G>A
- NM_001407679.1:c.3892G>A
- NM_001407680.1:c.3892G>A
- NM_001407681.1:c.3892G>A
- NM_001407682.1:c.3892G>A
- NM_001407683.1:c.3892G>A
- NM_001407684.1:c.4015G>A
- NM_001407685.1:c.3889G>A
- NM_001407686.1:c.3889G>A
- NM_001407687.1:c.3889G>A
- NM_001407688.1:c.3889G>A
- NM_001407689.1:c.3889G>A
- NM_001407690.1:c.3889G>A
- NM_001407691.1:c.3889G>A
- NM_001407692.1:c.3874G>A
- NM_001407694.1:c.3874G>A
- NM_001407695.1:c.3874G>A
- NM_001407696.1:c.3874G>A
- NM_001407697.1:c.3874G>A
- NM_001407698.1:c.3874G>A
- NM_001407724.1:c.3874G>A
- NM_001407725.1:c.3874G>A
- NM_001407726.1:c.3874G>A
- NM_001407727.1:c.3874G>A
- NM_001407728.1:c.3874G>A
- NM_001407729.1:c.3874G>A
- NM_001407730.1:c.3874G>A
- NM_001407731.1:c.3874G>A
- NM_001407732.1:c.3874G>A
- NM_001407733.1:c.3874G>A
- NM_001407734.1:c.3874G>A
- NM_001407735.1:c.3874G>A
- NM_001407736.1:c.3874G>A
- NM_001407737.1:c.3874G>A
- NM_001407738.1:c.3874G>A
- NM_001407739.1:c.3874G>A
- NM_001407740.1:c.3871G>A
- NM_001407741.1:c.3871G>A
- NM_001407742.1:c.3871G>A
- NM_001407743.1:c.3871G>A
- NM_001407744.1:c.3871G>A
- NM_001407745.1:c.3871G>A
- NM_001407746.1:c.3871G>A
- NM_001407747.1:c.3871G>A
- NM_001407748.1:c.3871G>A
- NM_001407749.1:c.3871G>A
- NM_001407750.1:c.3874G>A
- NM_001407751.1:c.3874G>A
- NM_001407752.1:c.3874G>A
- NM_001407838.1:c.3871G>A
- NM_001407839.1:c.3871G>A
- NM_001407841.1:c.3871G>A
- NM_001407842.1:c.3871G>A
- NM_001407843.1:c.3871G>A
- NM_001407844.1:c.3871G>A
- NM_001407845.1:c.3871G>A
- NM_001407846.1:c.3871G>A
- NM_001407847.1:c.3871G>A
- NM_001407848.1:c.3871G>A
- NM_001407849.1:c.3871G>A
- NM_001407850.1:c.3874G>A
- NM_001407851.1:c.3874G>A
- NM_001407852.1:c.3874G>A
- NM_001407853.1:c.3802G>A
- NM_001407854.1:c.4015G>A
- NM_001407858.1:c.4015G>A
- NM_001407859.1:c.4015G>A
- NM_001407860.1:c.4012G>A
- NM_001407861.1:c.4012G>A
- NM_001407862.1:c.3814G>A
- NM_001407863.1:c.3892G>A
- NM_001407874.1:c.3811G>A
- NM_001407875.1:c.3811G>A
- NM_001407879.1:c.3805G>A
- NM_001407881.1:c.3805G>A
- NM_001407882.1:c.3805G>A
- NM_001407884.1:c.3805G>A
- NM_001407885.1:c.3805G>A
- NM_001407886.1:c.3805G>A
- NM_001407887.1:c.3805G>A
- NM_001407889.1:c.3805G>A
- NM_001407894.1:c.3802G>A
- NM_001407895.1:c.3802G>A
- NM_001407896.1:c.3802G>A
- NM_001407897.1:c.3802G>A
- NM_001407898.1:c.3802G>A
- NM_001407899.1:c.3802G>A
- NM_001407900.1:c.3805G>A
- NM_001407902.1:c.3805G>A
- NM_001407904.1:c.3805G>A
- NM_001407906.1:c.3805G>A
- NM_001407907.1:c.3805G>A
- NM_001407908.1:c.3805G>A
- NM_001407909.1:c.3805G>A
- NM_001407910.1:c.3805G>A
- NM_001407915.1:c.3802G>A
- NM_001407916.1:c.3802G>A
- NM_001407917.1:c.3802G>A
- NM_001407918.1:c.3802G>A
- NM_001407919.1:c.3892G>A
- NM_001407920.1:c.3751G>A
- NM_001407921.1:c.3751G>A
- NM_001407922.1:c.3751G>A
- NM_001407923.1:c.3751G>A
- NM_001407924.1:c.3751G>A
- NM_001407925.1:c.3751G>A
- NM_001407926.1:c.3751G>A
- NM_001407927.1:c.3751G>A
- NM_001407928.1:c.3751G>A
- NM_001407929.1:c.3751G>A
- NM_001407930.1:c.3748G>A
- NM_001407931.1:c.3748G>A
- NM_001407932.1:c.3748G>A
- NM_001407933.1:c.3751G>A
- NM_001407934.1:c.3748G>A
- NM_001407935.1:c.3751G>A
- NM_001407936.1:c.3748G>A
- NM_001407937.1:c.3892G>A
- NM_001407938.1:c.3892G>A
- NM_001407939.1:c.3892G>A
- NM_001407940.1:c.3889G>A
- NM_001407941.1:c.3889G>A
- NM_001407942.1:c.3874G>A
- NM_001407943.1:c.3871G>A
- NM_001407944.1:c.3874G>A
- NM_001407945.1:c.3874G>A
- NM_001407946.1:c.3682G>A
- NM_001407947.1:c.3682G>A
- NM_001407948.1:c.3682G>A
- NM_001407949.1:c.3682G>A
- NM_001407950.1:c.3682G>A
- NM_001407951.1:c.3682G>A
- NM_001407952.1:c.3682G>A
- NM_001407953.1:c.3682G>A
- NM_001407954.1:c.3679G>A
- NM_001407955.1:c.3679G>A
- NM_001407956.1:c.3679G>A
- NM_001407957.1:c.3682G>A
- NM_001407958.1:c.3679G>A
- NM_001407959.1:c.3634G>A
- NM_001407960.1:c.3634G>A
- NM_001407962.1:c.3631G>A
- NM_001407963.1:c.3634G>A
- NM_001407964.1:c.3871G>A
- NM_001407965.1:c.3511G>A
- NM_001407966.1:c.3127G>A
- NM_001407967.1:c.3127G>A
- NM_001407968.1:c.1411G>A
- NM_001407969.1:c.1411G>A
- NM_001407970.1:c.788-484G>A
- NM_001407971.1:c.788-484G>A
- NM_001407972.1:c.785-484G>A
- NM_001407973.1:c.788-484G>A
- NM_001407974.1:c.788-484G>A
- NM_001407975.1:c.788-484G>A
- NM_001407976.1:c.788-484G>A
- NM_001407977.1:c.788-484G>A
- NM_001407978.1:c.788-484G>A
- NM_001407979.1:c.788-484G>A
- NM_001407980.1:c.788-484G>A
- NM_001407981.1:c.788-484G>A
- NM_001407982.1:c.788-484G>A
- NM_001407983.1:c.788-484G>A
- NM_001407984.1:c.785-484G>A
- NM_001407985.1:c.785-484G>A
- NM_001407986.1:c.785-484G>A
- NM_001407990.1:c.788-484G>A
- NM_001407991.1:c.785-484G>A
- NM_001407992.1:c.785-484G>A
- NM_001407993.1:c.788-484G>A
- NM_001408392.1:c.785-484G>A
- NM_001408396.1:c.785-484G>A
- NM_001408397.1:c.785-484G>A
- NM_001408398.1:c.785-484G>A
- NM_001408399.1:c.785-484G>A
- NM_001408400.1:c.785-484G>A
- NM_001408401.1:c.785-484G>A
- NM_001408402.1:c.785-484G>A
- NM_001408403.1:c.788-484G>A
- NM_001408404.1:c.788-484G>A
- NM_001408406.1:c.791-493G>A
- NM_001408407.1:c.785-484G>A
- NM_001408408.1:c.779-484G>A
- NM_001408409.1:c.710-484G>A
- NM_001408410.1:c.647-484G>A
- NM_001408411.1:c.710-484G>A
- NM_001408412.1:c.710-484G>A
- NM_001408413.1:c.707-484G>A
- NM_001408414.1:c.710-484G>A
- NM_001408415.1:c.710-484G>A
- NM_001408416.1:c.707-484G>A
- NM_001408418.1:c.671-484G>A
- NM_001408419.1:c.671-484G>A
- NM_001408420.1:c.671-484G>A
- NM_001408421.1:c.668-484G>A
- NM_001408422.1:c.671-484G>A
- NM_001408423.1:c.671-484G>A
- NM_001408424.1:c.668-484G>A
- NM_001408425.1:c.665-484G>A
- NM_001408426.1:c.665-484G>A
- NM_001408427.1:c.665-484G>A
- NM_001408428.1:c.665-484G>A
- NM_001408429.1:c.665-484G>A
- NM_001408430.1:c.665-484G>A
- NM_001408431.1:c.668-484G>A
- NM_001408432.1:c.662-484G>A
- NM_001408433.1:c.662-484G>A
- NM_001408434.1:c.662-484G>A
- NM_001408435.1:c.662-484G>A
- NM_001408436.1:c.665-484G>A
- NM_001408437.1:c.665-484G>A
- NM_001408438.1:c.665-484G>A
- NM_001408439.1:c.665-484G>A
- NM_001408440.1:c.665-484G>A
- NM_001408441.1:c.665-484G>A
- NM_001408442.1:c.665-484G>A
- NM_001408443.1:c.665-484G>A
- NM_001408444.1:c.665-484G>A
- NM_001408445.1:c.662-484G>A
- NM_001408446.1:c.662-484G>A
- NM_001408447.1:c.662-484G>A
- NM_001408448.1:c.662-484G>A
- NM_001408450.1:c.662-484G>A
- NM_001408451.1:c.653-484G>A
- NM_001408452.1:c.647-484G>A
- NM_001408453.1:c.647-484G>A
- NM_001408454.1:c.647-484G>A
- NM_001408455.1:c.647-484G>A
- NM_001408456.1:c.647-484G>A
- NM_001408457.1:c.647-484G>A
- NM_001408458.1:c.647-484G>A
- NM_001408459.1:c.647-484G>A
- NM_001408460.1:c.647-484G>A
- NM_001408461.1:c.647-484G>A
- NM_001408462.1:c.644-484G>A
- NM_001408463.1:c.644-484G>A
- NM_001408464.1:c.644-484G>A
- NM_001408465.1:c.644-484G>A
- NM_001408466.1:c.647-484G>A
- NM_001408467.1:c.647-484G>A
- NM_001408468.1:c.644-484G>A
- NM_001408469.1:c.647-484G>A
- NM_001408470.1:c.644-484G>A
- NM_001408472.1:c.788-484G>A
- NM_001408473.1:c.785-484G>A
- NM_001408474.1:c.587-484G>A
- NM_001408475.1:c.584-484G>A
- NM_001408476.1:c.587-484G>A
- NM_001408478.1:c.578-484G>A
- NM_001408479.1:c.578-484G>A
- NM_001408480.1:c.578-484G>A
- NM_001408481.1:c.578-484G>A
- NM_001408482.1:c.578-484G>A
- NM_001408483.1:c.578-484G>A
- NM_001408484.1:c.578-484G>A
- NM_001408485.1:c.578-484G>A
- NM_001408489.1:c.578-484G>A
- NM_001408490.1:c.575-484G>A
- NM_001408491.1:c.575-484G>A
- NM_001408492.1:c.578-484G>A
- NM_001408493.1:c.575-484G>A
- NM_001408494.1:c.548-484G>A
- NM_001408495.1:c.545-484G>A
- NM_001408496.1:c.524-484G>A
- NM_001408497.1:c.524-484G>A
- NM_001408498.1:c.524-484G>A
- NM_001408499.1:c.524-484G>A
- NM_001408500.1:c.524-484G>A
- NM_001408501.1:c.524-484G>A
- NM_001408502.1:c.455-484G>A
- NM_001408503.1:c.521-484G>A
- NM_001408504.1:c.521-484G>A
- NM_001408505.1:c.521-484G>A
- NM_001408506.1:c.461-484G>A
- NM_001408507.1:c.461-484G>A
- NM_001408508.1:c.452-484G>A
- NM_001408509.1:c.452-484G>A
- NM_001408510.1:c.407-484G>A
- NM_001408511.1:c.404-484G>A
- NM_001408512.1:c.284-484G>A
- NM_001408513.1:c.578-484G>A
- NM_001408514.1:c.578-484G>A
- NM_007294.4:c.4015G>AMANE SELECT
- NM_007297.4:c.3874G>A
- NM_007298.4:c.788-484G>A
- NM_007299.4:c.788-484G>A
- NM_007300.4:c.4015G>A
- NP_001394500.1:p.Glu1268Lys
- NP_001394510.1:p.Glu1339Lys
- NP_001394511.1:p.Glu1339Lys
- NP_001394512.1:p.Glu1339Lys
- NP_001394514.1:p.Glu1339Lys
- NP_001394516.1:p.Glu1338Lys
- NP_001394519.1:p.Glu1338Lys
- NP_001394520.1:p.Glu1338Lys
- NP_001394522.1:p.Glu1339Lys
- NP_001394523.1:p.Glu1339Lys
- NP_001394525.1:p.Glu1339Lys
- NP_001394526.1:p.Glu1339Lys
- NP_001394527.1:p.Glu1339Lys
- NP_001394531.1:p.Glu1339Lys
- NP_001394532.1:p.Glu1339Lys
- NP_001394534.1:p.Glu1339Lys
- NP_001394539.1:p.Glu1338Lys
- NP_001394540.1:p.Glu1338Lys
- NP_001394541.1:p.Glu1338Lys
- NP_001394542.1:p.Glu1338Lys
- NP_001394543.1:p.Glu1338Lys
- NP_001394544.1:p.Glu1338Lys
- NP_001394545.1:p.Glu1339Lys
- NP_001394546.1:p.Glu1339Lys
- NP_001394547.1:p.Glu1339Lys
- NP_001394548.1:p.Glu1339Lys
- NP_001394549.1:p.Glu1339Lys
- NP_001394550.1:p.Glu1339Lys
- NP_001394551.1:p.Glu1339Lys
- NP_001394552.1:p.Glu1339Lys
- NP_001394553.1:p.Glu1339Lys
- NP_001394554.1:p.Glu1339Lys
- NP_001394555.1:p.Glu1339Lys
- NP_001394556.1:p.Glu1338Lys
- NP_001394557.1:p.Glu1338Lys
- NP_001394558.1:p.Glu1338Lys
- NP_001394559.1:p.Glu1338Lys
- NP_001394560.1:p.Glu1338Lys
- NP_001394561.1:p.Glu1338Lys
- NP_001394562.1:p.Glu1338Lys
- NP_001394563.1:p.Glu1338Lys
- NP_001394564.1:p.Glu1338Lys
- NP_001394565.1:p.Glu1338Lys
- NP_001394566.1:p.Glu1338Lys
- NP_001394567.1:p.Glu1338Lys
- NP_001394568.1:p.Glu1339Lys
- NP_001394569.1:p.Glu1339Lys
- NP_001394570.1:p.Glu1339Lys
- NP_001394571.1:p.Glu1339Lys
- NP_001394573.1:p.Glu1338Lys
- NP_001394574.1:p.Glu1338Lys
- NP_001394575.1:p.Glu1336Lys
- NP_001394576.1:p.Glu1336Lys
- NP_001394577.1:p.Glu1298Lys
- NP_001394578.1:p.Glu1297Lys
- NP_001394581.1:p.Glu1339Lys
- NP_001394582.1:p.Glu1313Lys
- NP_001394583.1:p.Glu1313Lys
- NP_001394584.1:p.Glu1313Lys
- NP_001394585.1:p.Glu1313Lys
- NP_001394586.1:p.Glu1313Lys
- NP_001394587.1:p.Glu1313Lys
- NP_001394588.1:p.Glu1312Lys
- NP_001394589.1:p.Glu1312Lys
- NP_001394590.1:p.Glu1312Lys
- NP_001394591.1:p.Glu1312Lys
- NP_001394592.1:p.Glu1313Lys
- NP_001394593.1:p.Glu1298Lys
- NP_001394594.1:p.Glu1298Lys
- NP_001394595.1:p.Glu1298Lys
- NP_001394596.1:p.Glu1298Lys
- NP_001394597.1:p.Glu1298Lys
- NP_001394598.1:p.Glu1298Lys
- NP_001394599.1:p.Glu1297Lys
- NP_001394600.1:p.Glu1297Lys
- NP_001394601.1:p.Glu1297Lys
- NP_001394602.1:p.Glu1297Lys
- NP_001394603.1:p.Glu1298Lys
- NP_001394604.1:p.Glu1298Lys
- NP_001394605.1:p.Glu1298Lys
- NP_001394606.1:p.Glu1298Lys
- NP_001394607.1:p.Glu1298Lys
- NP_001394608.1:p.Glu1298Lys
- NP_001394609.1:p.Glu1298Lys
- NP_001394610.1:p.Glu1298Lys
- NP_001394611.1:p.Glu1298Lys
- NP_001394612.1:p.Glu1298Lys
- NP_001394613.1:p.Glu1339Lys
- NP_001394614.1:p.Glu1297Lys
- NP_001394615.1:p.Glu1297Lys
- NP_001394616.1:p.Glu1297Lys
- NP_001394617.1:p.Glu1297Lys
- NP_001394618.1:p.Glu1297Lys
- NP_001394619.1:p.Glu1297Lys
- NP_001394620.1:p.Glu1297Lys
- NP_001394621.1:p.Glu1292Lys
- NP_001394623.1:p.Glu1292Lys
- NP_001394624.1:p.Glu1292Lys
- NP_001394625.1:p.Glu1292Lys
- NP_001394626.1:p.Glu1292Lys
- NP_001394627.1:p.Glu1292Lys
- NP_001394653.1:p.Glu1292Lys
- NP_001394654.1:p.Glu1292Lys
- NP_001394655.1:p.Glu1292Lys
- NP_001394656.1:p.Glu1292Lys
- NP_001394657.1:p.Glu1292Lys
- NP_001394658.1:p.Glu1292Lys
- NP_001394659.1:p.Glu1292Lys
- NP_001394660.1:p.Glu1292Lys
- NP_001394661.1:p.Glu1292Lys
- NP_001394662.1:p.Glu1292Lys
- NP_001394663.1:p.Glu1292Lys
- NP_001394664.1:p.Glu1292Lys
- NP_001394665.1:p.Glu1292Lys
- NP_001394666.1:p.Glu1292Lys
- NP_001394667.1:p.Glu1292Lys
- NP_001394668.1:p.Glu1292Lys
- NP_001394669.1:p.Glu1291Lys
- NP_001394670.1:p.Glu1291Lys
- NP_001394671.1:p.Glu1291Lys
- NP_001394672.1:p.Glu1291Lys
- NP_001394673.1:p.Glu1291Lys
- NP_001394674.1:p.Glu1291Lys
- NP_001394675.1:p.Glu1291Lys
- NP_001394676.1:p.Glu1291Lys
- NP_001394677.1:p.Glu1291Lys
- NP_001394678.1:p.Glu1291Lys
- NP_001394679.1:p.Glu1292Lys
- NP_001394680.1:p.Glu1292Lys
- NP_001394681.1:p.Glu1292Lys
- NP_001394767.1:p.Glu1291Lys
- NP_001394768.1:p.Glu1291Lys
- NP_001394770.1:p.Glu1291Lys
- NP_001394771.1:p.Glu1291Lys
- NP_001394772.1:p.Glu1291Lys
- NP_001394773.1:p.Glu1291Lys
- NP_001394774.1:p.Glu1291Lys
- NP_001394775.1:p.Glu1291Lys
- NP_001394776.1:p.Glu1291Lys
- NP_001394777.1:p.Glu1291Lys
- NP_001394778.1:p.Glu1291Lys
- NP_001394779.1:p.Glu1292Lys
- NP_001394780.1:p.Glu1292Lys
- NP_001394781.1:p.Glu1292Lys
- NP_001394782.1:p.Glu1268Lys
- NP_001394783.1:p.Glu1339Lys
- NP_001394787.1:p.Glu1339Lys
- NP_001394788.1:p.Glu1339Lys
- NP_001394789.1:p.Glu1338Lys
- NP_001394790.1:p.Glu1338Lys
- NP_001394791.1:p.Glu1272Lys
- NP_001394792.1:p.Glu1298Lys
- NP_001394803.1:p.Glu1271Lys
- NP_001394804.1:p.Glu1271Lys
- NP_001394808.1:p.Glu1269Lys
- NP_001394810.1:p.Glu1269Lys
- NP_001394811.1:p.Glu1269Lys
- NP_001394813.1:p.Glu1269Lys
- NP_001394814.1:p.Glu1269Lys
- NP_001394815.1:p.Glu1269Lys
- NP_001394816.1:p.Glu1269Lys
- NP_001394818.1:p.Glu1269Lys
- NP_001394823.1:p.Glu1268Lys
- NP_001394824.1:p.Glu1268Lys
- NP_001394825.1:p.Glu1268Lys
- NP_001394826.1:p.Glu1268Lys
- NP_001394827.1:p.Glu1268Lys
- NP_001394828.1:p.Glu1268Lys
- NP_001394829.1:p.Glu1269Lys
- NP_001394831.1:p.Glu1269Lys
- NP_001394833.1:p.Glu1269Lys
- NP_001394835.1:p.Glu1269Lys
- NP_001394836.1:p.Glu1269Lys
- NP_001394837.1:p.Glu1269Lys
- NP_001394838.1:p.Glu1269Lys
- NP_001394839.1:p.Glu1269Lys
- NP_001394844.1:p.Glu1268Lys
- NP_001394845.1:p.Glu1268Lys
- NP_001394846.1:p.Glu1268Lys
- NP_001394847.1:p.Glu1268Lys
- NP_001394848.1:p.Glu1298Lys
- NP_001394849.1:p.Glu1251Lys
- NP_001394850.1:p.Glu1251Lys
- NP_001394851.1:p.Glu1251Lys
- NP_001394852.1:p.Glu1251Lys
- NP_001394853.1:p.Glu1251Lys
- NP_001394854.1:p.Glu1251Lys
- NP_001394855.1:p.Glu1251Lys
- NP_001394856.1:p.Glu1251Lys
- NP_001394857.1:p.Glu1251Lys
- NP_001394858.1:p.Glu1251Lys
- NP_001394859.1:p.Glu1250Lys
- NP_001394860.1:p.Glu1250Lys
- NP_001394861.1:p.Glu1250Lys
- NP_001394862.1:p.Glu1251Lys
- NP_001394863.1:p.Glu1250Lys
- NP_001394864.1:p.Glu1251Lys
- NP_001394865.1:p.Glu1250Lys
- NP_001394866.1:p.Glu1298Lys
- NP_001394867.1:p.Glu1298Lys
- NP_001394868.1:p.Glu1298Lys
- NP_001394869.1:p.Glu1297Lys
- NP_001394870.1:p.Glu1297Lys
- NP_001394871.1:p.Glu1292Lys
- NP_001394872.1:p.Glu1291Lys
- NP_001394873.1:p.Glu1292Lys
- NP_001394874.1:p.Glu1292Lys
- NP_001394875.1:p.Glu1228Lys
- NP_001394876.1:p.Glu1228Lys
- NP_001394877.1:p.Glu1228Lys
- NP_001394878.1:p.Glu1228Lys
- NP_001394879.1:p.Glu1228Lys
- NP_001394880.1:p.Glu1228Lys
- NP_001394881.1:p.Glu1228Lys
- NP_001394882.1:p.Glu1228Lys
- NP_001394883.1:p.Glu1227Lys
- NP_001394884.1:p.Glu1227Lys
- NP_001394885.1:p.Glu1227Lys
- NP_001394886.1:p.Glu1228Lys
- NP_001394887.1:p.Glu1227Lys
- NP_001394888.1:p.Glu1212Lys
- NP_001394889.1:p.Glu1212Lys
- NP_001394891.1:p.Glu1211Lys
- NP_001394892.1:p.Glu1212Lys
- NP_001394893.1:p.Glu1291Lys
- NP_001394894.1:p.Glu1171Lys
- NP_001394895.1:p.Glu1043Lys
- NP_001394896.1:p.Glu1043Lys
- NP_001394897.1:p.Glu471Lys
- NP_001394898.1:p.Glu471Lys
- NP_009225.1:p.Glu1339Lys
- NP_009225.1:p.Glu1339Lys
- NP_009228.2:p.Glu1292Lys
- NP_009231.2:p.Glu1339Lys
- LRG_292t1:c.4015G>A
- LRG_292:g.126468G>A
- LRG_292p1:p.Glu1339Lys
- NC_000017.10:g.41243533C>T
- NM_007294.3:c.4015G>A
- NR_027676.1:n.4151G>A
This HGVS expression did not pass validation- Protein change:
- E1043K
- Links:
- dbSNP: rs80357021
- NCBI 1000 Genomes Browser:
- rs80357021
- Molecular consequence:
- NM_001407970.1:c.788-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407971.1:c.788-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407972.1:c.785-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407973.1:c.788-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407974.1:c.788-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407975.1:c.788-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407976.1:c.788-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407977.1:c.788-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407978.1:c.788-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407979.1:c.788-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407980.1:c.788-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407981.1:c.788-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407982.1:c.788-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407983.1:c.788-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407984.1:c.785-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407985.1:c.785-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407986.1:c.785-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407990.1:c.788-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407991.1:c.785-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407992.1:c.785-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407993.1:c.788-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408392.1:c.785-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408396.1:c.785-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408397.1:c.785-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408398.1:c.785-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408399.1:c.785-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408400.1:c.785-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408401.1:c.785-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408402.1:c.785-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408403.1:c.788-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408404.1:c.788-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408406.1:c.791-493G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408407.1:c.785-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408408.1:c.779-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408409.1:c.710-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408410.1:c.647-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408411.1:c.710-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408412.1:c.710-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408413.1:c.707-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408414.1:c.710-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408415.1:c.710-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408416.1:c.707-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408418.1:c.671-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408419.1:c.671-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408420.1:c.671-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408421.1:c.668-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408422.1:c.671-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408423.1:c.671-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408424.1:c.668-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408425.1:c.665-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408426.1:c.665-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408427.1:c.665-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408428.1:c.665-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408429.1:c.665-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408430.1:c.665-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408431.1:c.668-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408432.1:c.662-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408433.1:c.662-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408434.1:c.662-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408435.1:c.662-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408436.1:c.665-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408437.1:c.665-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408438.1:c.665-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408439.1:c.665-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408440.1:c.665-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408441.1:c.665-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408442.1:c.665-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408443.1:c.665-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408444.1:c.665-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408445.1:c.662-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408446.1:c.662-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408447.1:c.662-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408448.1:c.662-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408450.1:c.662-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408451.1:c.653-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408452.1:c.647-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408453.1:c.647-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408454.1:c.647-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408455.1:c.647-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408456.1:c.647-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408457.1:c.647-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408458.1:c.647-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408459.1:c.647-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408460.1:c.647-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408461.1:c.647-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408462.1:c.644-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408463.1:c.644-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408464.1:c.644-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408465.1:c.644-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408466.1:c.647-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408467.1:c.647-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408468.1:c.644-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408469.1:c.647-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408470.1:c.644-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408472.1:c.788-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408473.1:c.785-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408474.1:c.587-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408475.1:c.584-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408476.1:c.587-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408478.1:c.578-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408479.1:c.578-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408480.1:c.578-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408481.1:c.578-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408482.1:c.578-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408483.1:c.578-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408484.1:c.578-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408485.1:c.578-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408489.1:c.578-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408490.1:c.575-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408491.1:c.575-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408492.1:c.578-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408493.1:c.575-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408494.1:c.548-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408495.1:c.545-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408496.1:c.524-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408497.1:c.524-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408498.1:c.524-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408499.1:c.524-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408500.1:c.524-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408501.1:c.524-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408502.1:c.455-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408503.1:c.521-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408504.1:c.521-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408505.1:c.521-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408506.1:c.461-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408507.1:c.461-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408508.1:c.452-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408509.1:c.452-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408510.1:c.407-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408511.1:c.404-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408512.1:c.284-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408513.1:c.578-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408514.1:c.578-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_007298.4:c.788-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_007299.4:c.788-484G>A - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407571.1:c.3802G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407581.1:c.4015G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407582.1:c.4015G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407583.1:c.4015G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407585.1:c.4015G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407587.1:c.4012G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407590.1:c.4012G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407591.1:c.4012G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407593.1:c.4015G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407594.1:c.4015G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407596.1:c.4015G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407597.1:c.4015G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407598.1:c.4015G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407602.1:c.4015G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407603.1:c.4015G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407605.1:c.4015G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407610.1:c.4012G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407611.1:c.4012G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407612.1:c.4012G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407613.1:c.4012G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407614.1:c.4012G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407615.1:c.4012G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407616.1:c.4015G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407617.1:c.4015G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407618.1:c.4015G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407619.1:c.4015G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407620.1:c.4015G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407621.1:c.4015G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407622.1:c.4015G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407623.1:c.4015G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407624.1:c.4015G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407625.1:c.4015G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407626.1:c.4015G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407627.1:c.4012G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407628.1:c.4012G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407629.1:c.4012G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407630.1:c.4012G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407631.1:c.4012G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407632.1:c.4012G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407633.1:c.4012G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407634.1:c.4012G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407635.1:c.4012G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407636.1:c.4012G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407637.1:c.4012G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407638.1:c.4012G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407639.1:c.4015G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407640.1:c.4015G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407641.1:c.4015G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407642.1:c.4015G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407644.1:c.4012G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407645.1:c.4012G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407646.1:c.4006G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407647.1:c.4006G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407648.1:c.3892G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407649.1:c.3889G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407652.1:c.4015G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407653.1:c.3937G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407654.1:c.3937G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407655.1:c.3937G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407656.1:c.3937G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407657.1:c.3937G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407658.1:c.3937G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407659.1:c.3934G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407660.1:c.3934G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407661.1:c.3934G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407662.1:c.3934G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407663.1:c.3937G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407664.1:c.3892G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407665.1:c.3892G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407666.1:c.3892G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407667.1:c.3892G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407668.1:c.3892G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407669.1:c.3892G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407670.1:c.3889G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407671.1:c.3889G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407672.1:c.3889G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407673.1:c.3889G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407674.1:c.3892G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407675.1:c.3892G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407676.1:c.3892G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407677.1:c.3892G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407678.1:c.3892G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407679.1:c.3892G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407680.1:c.3892G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407681.1:c.3892G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407682.1:c.3892G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407683.1:c.3892G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407684.1:c.4015G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407685.1:c.3889G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407686.1:c.3889G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407687.1:c.3889G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407688.1:c.3889G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407689.1:c.3889G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407690.1:c.3889G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407691.1:c.3889G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407692.1:c.3874G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407694.1:c.3874G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407695.1:c.3874G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407696.1:c.3874G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407697.1:c.3874G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407698.1:c.3874G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407724.1:c.3874G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407725.1:c.3874G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407726.1:c.3874G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407727.1:c.3874G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407728.1:c.3874G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407729.1:c.3874G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407730.1:c.3874G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407731.1:c.3874G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407732.1:c.3874G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407733.1:c.3874G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407734.1:c.3874G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407735.1:c.3874G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407736.1:c.3874G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407737.1:c.3874G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407738.1:c.3874G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407739.1:c.3874G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407740.1:c.3871G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407741.1:c.3871G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407742.1:c.3871G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407743.1:c.3871G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407744.1:c.3871G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407745.1:c.3871G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407746.1:c.3871G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407747.1:c.3871G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407748.1:c.3871G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407749.1:c.3871G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407750.1:c.3874G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407751.1:c.3874G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407752.1:c.3874G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407838.1:c.3871G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407839.1:c.3871G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407841.1:c.3871G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407842.1:c.3871G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407843.1:c.3871G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407844.1:c.3871G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407845.1:c.3871G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407846.1:c.3871G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407847.1:c.3871G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407848.1:c.3871G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407849.1:c.3871G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407850.1:c.3874G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407851.1:c.3874G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407852.1:c.3874G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407853.1:c.3802G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407854.1:c.4015G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407858.1:c.4015G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407859.1:c.4015G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407860.1:c.4012G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407861.1:c.4012G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407862.1:c.3814G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407863.1:c.3892G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407874.1:c.3811G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407875.1:c.3811G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407879.1:c.3805G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407881.1:c.3805G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407882.1:c.3805G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407884.1:c.3805G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407885.1:c.3805G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407886.1:c.3805G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407887.1:c.3805G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407889.1:c.3805G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407894.1:c.3802G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407895.1:c.3802G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407896.1:c.3802G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407897.1:c.3802G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407898.1:c.3802G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407899.1:c.3802G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407900.1:c.3805G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407902.1:c.3805G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407904.1:c.3805G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407906.1:c.3805G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407907.1:c.3805G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407908.1:c.3805G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407909.1:c.3805G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407910.1:c.3805G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407915.1:c.3802G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407916.1:c.3802G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407917.1:c.3802G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407918.1:c.3802G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407919.1:c.3892G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407920.1:c.3751G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407921.1:c.3751G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407922.1:c.3751G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407923.1:c.3751G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407924.1:c.3751G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407925.1:c.3751G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407926.1:c.3751G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407927.1:c.3751G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407928.1:c.3751G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407929.1:c.3751G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407930.1:c.3748G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407931.1:c.3748G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407932.1:c.3748G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407933.1:c.3751G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407934.1:c.3748G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407935.1:c.3751G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407936.1:c.3748G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407937.1:c.3892G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407938.1:c.3892G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407939.1:c.3892G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407940.1:c.3889G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407941.1:c.3889G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407942.1:c.3874G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407943.1:c.3871G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407944.1:c.3874G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407945.1:c.3874G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407946.1:c.3682G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407947.1:c.3682G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407948.1:c.3682G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407949.1:c.3682G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407950.1:c.3682G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407951.1:c.3682G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407952.1:c.3682G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407953.1:c.3682G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407954.1:c.3679G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407955.1:c.3679G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407956.1:c.3679G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407957.1:c.3682G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407958.1:c.3679G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407959.1:c.3634G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407960.1:c.3634G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407962.1:c.3631G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407963.1:c.3634G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407964.1:c.3871G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407965.1:c.3511G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407966.1:c.3127G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407967.1:c.3127G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407968.1:c.1411G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_001407969.1:c.1411G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_007294.4:c.4015G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_007297.4:c.3874G>A - missense variant - [Sequence Ontology: SO:0001583]
- NM_007300.4:c.4015G>A - missense variant - [Sequence Ontology: SO:0001583]
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
gp160, partial [HIV-1 CRF01_AE]
gp160, partial [HIV-1 CRF01_AE]gi|283483030|emb|CAR96223.1|Protein
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See more...Assertion and evidence details
Submission Accession | Submitter | Review Status (Assertion method) | Clinical Significance (Last evaluated) | Origin | Method | Citations |
---|---|---|---|---|---|---|
SCV000210163 | GeneDx | criteria provided, single submitter (GeneDx Variant Classification (06012015)) | Uncertain significance (Aug 12, 2014) | germline | clinical testing |
Summary from all submissions
Ethnicity | Origin | Affected | Individuals | Families | Chromosomes tested | Number Tested | Family history | Method |
---|---|---|---|---|---|---|---|---|
not provided | germline | yes | not provided | not provided | not provided | not provided | not provided | clinical testing |
Details of each submission
From GeneDx, SCV000210163.10
# | Ethnicity | Individuals | Chromosomes Tested | Family History | Method | Citations |
---|---|---|---|---|---|---|
1 | not provided | not provided | not provided | not provided | clinical testing | not provided |
Description
This variant is denoted BRCA1 c.4015G>A at the cDNA level, p.Glu1339Lys (E1339K) at the protein level, and results in the change of a Glutamic Acid to a Lysine (GAA>AAA). This variant has not, to our knowledge, been published in the literature as pathogenic or benign. BRCA1 Glu1339Lys was not observed in approximately 6,500 individuals of European and African American ancestry in the NHLBI Exome Sequencing Project, indicating it is not a common benign variant in these populations. Since Glutamic Acid and Lysine differ in polarity, charge, size or other properties, this is considered a non-conservative amino acid substitution. BRCA1 Glu1339Lys occurs at a position that is well conserved across mammals and is located within the SQ/TQ cluster domain (SCD), a region with preferred sites of phosphorylation by the ATM protein as well as the region of interaction with ATM, CHK2 and CDK2 (Narod 2004, Roy 2012). In silico analyses predict that this variant is unlikely to alter protein structure or function. Based on currently available information, it is unclear whether BRCA1 Glu1339Lys is pathogenic or benign. We consider it to be a variant of uncertain significance.
# | Sample | Method | Observation | |||||||
---|---|---|---|---|---|---|---|---|---|---|
Origin | Affected | Number tested | Tissue | Purpose | Method | Individuals | Allele frequency | Families | Co-occurrences | |
1 | germline | yes | not provided | not provided | not provided | not provided | not provided | not provided | not provided |
Last Updated: Sep 29, 2024