Related gene-specific medical variations for Gene (Select 57491) - ClinVar

Links from Gene

Items: 82

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3278827	NM_001377236.1(AHRR):c.490C>T (p.Arg164Cys)	AHRR, PDCD6-AHRR (R164C)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3278819	NM_001377236.1(AHRR):c.76G>C (p.Gly26Arg)	AHRR, PDCD6-AHRR (G26R)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3278812	NM_001377236.1(AHRR):c.947A>C (p.His316Pro)	AHRR, PDCD6-AHRR (H316P)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3278802	NM_001377236.1(AHRR):c.634G>A (p.Glu212Lys)	AHRR, PDCD6-AHRR (E212K)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3278792	NM_001377236.1(AHRR):c.1910G>A (p.Arg637Gln)	AHRR, PDCD6-AHRR (R637Q)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3278782	NM_001377236.1(AHRR):c.1046C>G (p.Ala349Gly)	AHRR, PDCD6-AHRR (A349G)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3278771	NM_001377236.1(AHRR):c.1954G>A (p.Ala652Thr)	AHRR, PDCD6-AHRR (A652T)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign
Select item 3278763	NM_001377236.1(AHRR):c.1918G>A (p.Gly640Ser)	AHRR, PDCD6-AHRR (G640S)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3278756	NM_001377236.1(AHRR):c.109C>T (p.Arg37Trp)	AHRR, PDCD6-AHRR (R37W)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3278739	NM_001377236.1(AHRR):c.592A>T (p.Arg198Trp)	AHRR, PDCD6-AHRR (R198W)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3102334	NM_001377236.1(AHRR):c.787C>T (p.Arg263Trp)	AHRR, PDCD6-AHRR (R263W)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3102326	NM_001377236.1(AHRR):c.709-143C>T	AHRR, PDCD6-AHRR	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3102307	NM_001377236.1(AHRR):c.392C>T (p.Thr131Met)	AHRR, LOC108251796 +1 more (T131M)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign
Select item 3102297	NM_001377236.1(AHRR):c.283G>A (p.Ala95Thr)	AHRR, PDCD6-AHRR (A95T)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3102286	NM_001377236.1(AHRR):c.2074G>C (p.Gly692Arg)	AHRR, PDCD6-AHRR (G692R)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3102248	NM_001377236.1(AHRR):c.1736G>A (p.Arg579Gln)	AHRR, PDCD6-AHRR (R579Q)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3102229	NM_001377236.1(AHRR):c.1544T>G (p.Val515Gly)	AHRR, PDCD6-AHRR (V515G)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3102221	NM_001377236.1(AHRR):c.1375G>A (p.Ala459Thr)	AHRR, PDCD6-AHRR (A459T)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3102217	NM_001377236.1(AHRR):c.1280G>T (p.Arg427Leu)	AHRR, PDCD6-AHRR (R427L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3102210	NM_001377236.1(AHRR):c.1280G>A (p.Arg427His)	AHRR, PDCD6-AHRR (R427H)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3102192	NM_001377236.1(AHRR):c.104G>A (p.Arg35Gln)	AHRR, PDCD6-AHRR (R35Q)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3102164	NM_001377236.1(AHRR):c.994G>T (p.Val332Phe)	AHRR, PDCD6-AHRR (V332F)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3102155	NM_001377236.1(AHRR):c.88T>C (p.Ser30Pro)	AHRR, PDCD6-AHRR (S30P)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2685143	GRCh37/hg19 5p15.33(chr5:355319-408418)x1	AHRR	Copy number loss	not provided	GUncertain significance
Select item 2655247	NM_001377236.1(AHRR):c.1314G>A (p.Pro438=)	AHRR, PDCD6-AHRR	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 2655246	NM_001377236.1(AHRR):c.1020C>T (p.Asp340=)	AHRR, PDCD6-AHRR	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 2655245	NM_001377236.1(AHRR):c.981C>T (p.Ser327=)	AHRR, PDCD6-AHRR	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 2655244	NM_001377236.1(AHRR):c.706C>T (p.Leu236=)	AHRR, PDCD6-AHRR	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 2655243	NM_001377236.1(AHRR):c.414G>A (p.Thr138=)	AHRR, LOC108251796 +1 more	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 2616418	NM_001377236.1(AHRR):c.1606G>A (p.Glu536Lys)	AHRR, PDCD6-AHRR (E536K)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2614233	NM_001377236.1(AHRR):c.832G>A (p.Ala278Thr)	AHRR, PDCD6-AHRR (A278T)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign
Select item 2595275	NM_001377236.1(AHRR):c.116G>T (p.Arg39Leu)	AHRR, PDCD6-AHRR (R39L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2558799	NM_001377236.1(AHRR):c.1995G>C (p.Trp665Cys)	AHRR, PDCD6-AHRR (W665C)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2539030	NM_001377236.1(AHRR):c.959A>G (p.Asn320Ser)	AHRR, PDCD6-AHRR (N320S)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign
Select item 2532718	NM_001377236.1(AHRR):c.1877C>T (p.Pro626Leu)	AHRR, PDCD6-AHRR (P626L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2523721	NM_001377236.1(AHRR):c.2060C>T (p.Pro687Leu)	AHRR, PDCD6-AHRR (P687L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2519240	NM_001377236.1(AHRR):c.1117A>G (p.Arg373Gly)	AHRR, PDCD6-AHRR (R373G)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2508527	NM_001377236.1(AHRR):c.1069C>T (p.Arg357Trp)	AHRR, PDCD6-AHRR (R357W)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2507706	NM_001377236.1(AHRR):c.73G>A (p.Val25Met)	AHRR, PDCD6-AHRR (V25M)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2493705	NM_001377236.1(AHRR):c.311T>C (p.Leu104Pro)	AHRR, PDCD6-AHRR (L104P)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2470724	NM_001377236.1(AHRR):c.1774C>T (p.Arg592Trp)	AHRR, PDCD6-AHRR (R592W)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2469734	NM_001377236.1(AHRR):c.2072C>T (p.Ser691Leu)	AHRR, PDCD6-AHRR (S691L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2462258	NM_001377236.1(AHRR):c.1063T>G (p.Cys355Gly)	AHRR, PDCD6-AHRR (C355G)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2456970	NM_001377236.1(AHRR):c.196G>A (p.Val66Ile)	AHRR, PDCD6-AHRR (V66I)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2401820	NM_001377236.1(AHRR):c.1883C>T (p.Ser628Leu)	AHRR, PDCD6-AHRR (S628L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2396756	NM_001377236.1(AHRR):c.1495C>T (p.Arg499Cys)	AHRR, PDCD6-AHRR (R499C)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2371334	NM_001377236.1(AHRR):c.1268C>T (p.Pro423Leu)	AHRR, PDCD6-AHRR (P423L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign
Select item 2358749	NM_001377236.1(AHRR):c.626C>T (p.Thr209Met)	AHRR, PDCD6-AHRR (T209M)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2353873	NM_001377236.1(AHRR):c.709-166G>A	AHRR, PDCD6-AHRR	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2347249	NM_001377236.1(AHRR):c.778C>T (p.Leu260Phe)	AHRR, PDCD6-AHRR (L260F)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2346676	NM_001377236.1(AHRR):c.310C>G (p.Leu104Val)	AHRR, PDCD6-AHRR (L104V)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2340859	NM_001377236.1(AHRR):c.709-131C>G	AHRR, PDCD6-AHRR	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2340121	NM_001377236.1(AHRR):c.413C>T (p.Thr138Met)	AHRR, LOC108251796 +1 more (T138M)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2329849	NM_001377236.1(AHRR):c.546T>G (p.Phe182Leu)	AHRR, PDCD6-AHRR (F182L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2325321	NM_001377236.1(AHRR):c.325G>A (p.Val109Met)	AHRR, PDCD6-AHRR (V109M)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2321172	NM_001377236.1(AHRR):c.116G>A (p.Arg39His)	AHRR, PDCD6-AHRR (R39H)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2307968	NM_001377236.1(AHRR):c.1036C>A (p.Gln346Lys)	AHRR, PDCD6-AHRR (Q346K)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2306542	NM_001377236.1(AHRR):c.698C>T (p.Ser233Leu)	AHRR, PDCD6-AHRR (S233L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2300780	NM_001377236.1(AHRR):c.1999A>G (p.Thr667Ala)	AHRR, PDCD6-AHRR (T667A)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign
Select item 2299121	NM_001377236.1(AHRR):c.2047G>T (p.Ala683Ser)	AHRR, PDCD6-AHRR (A683S)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2289820	NM_001377236.1(AHRR):c.2087T>G (p.Leu696Arg)	AHRR, PDCD6-AHRR (L696R)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2284289	NM_001377236.1(AHRR):c.1844A>G (p.His615Arg)	AHRR, PDCD6-AHRR (H615R)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2272112	NM_001377236.1(AHRR):c.125C>G (p.Ala42Gly)	AHRR, PDCD6-AHRR (A42G)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2263981	NM_001377236.1(AHRR):c.1232G>A (p.Gly411Asp)	AHRR, PDCD6-AHRR (G411D)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2256741	NM_001377236.1(AHRR):c.502T>C (p.Cys168Arg)	AHRR, PDCD6-AHRR (C168R)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2251422	NM_001377236.1(AHRR):c.1768G>A (p.Gly590Ser)	AHRR, PDCD6-AHRR (G590S)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2242035	NM_001377236.1(AHRR):c.1285A>C (p.Met429Leu)	AHRR, PDCD6-AHRR (M429L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2236686	NM_001377236.1(AHRR):c.275C>T (p.Ala92Val)	AHRR, PDCD6-AHRR (A92V)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2229762	NM_001377236.1(AHRR):c.1727C>A (p.Pro576Gln)	AHRR, PDCD6-AHRR (P576Q)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2224946	NM_001377236.1(AHRR):c.247G>A (p.Val83Met)	AHRR, PDCD6-AHRR (V83M)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2223318	NM_001377236.1(AHRR):c.1561G>T (p.Asp521Tyr)	AHRR, PDCD6-AHRR (D521Y)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2216864	NM_001377236.1(AHRR):c.1613A>C (p.Asp538Ala)	AHRR, PDCD6-AHRR (D538A)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2216411	NM_001377236.1(AHRR):c.1168C>T (p.Arg390Trp)	AHRR, PDCD6-AHRR (R390W)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2215698	NM_001377236.1(AHRR):c.1670C>T (p.Ala557Val)	AHRR, PDCD6-AHRR (A557V)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 1297626	NM_001377236.1(AHRR):c.1113-1G>A	AHRR, PDCD6-AHRR	Single nucleotide variant (splice acceptor variant)	not provided	GUncertain significance
Select item 778862	NM_020731.4(AHRR):c.516C>T (p.Cys172=)	AHRR, PDCD6-AHRR	Single nucleotide variant	not provided	GBenign
Select item 769643	NM_020731.4(AHRR):c.1357C>T (p.Arg453Cys)	AHRR, PDCD6-AHRR	Single nucleotide variant	not provided	GBenign
Select item 738466	NM_020731.4(AHRR):c.1431G>C (p.Pro477=)	AHRR, PDCD6-AHRR	Single nucleotide variant	not provided	GLikely benign
Select item 726872	NM_020731.4(AHRR):c.168G>A (p.Pro56=)	AHRR, PDCD6-AHRR	Single nucleotide variant	not provided	GLikely benign
Select item 708922	NC_000005.10:g.434169C>T	AHRR, PDCD6-AHRR	Single nucleotide variant	not provided	GBenign/Likely benign
Select item 219350	NM_020731.4(AHRR):c.1472G>A (p.Arg491Gln)	AHRR, PDCD6-AHRR	Single nucleotide variant	Malignant tumor of prostate	GUncertain significance
Select item 145222	GRCh38/hg38 5p15.33(chr5:346162-404606)x3	AHRR, LOC126807281 +14 more	Copy number gain	See cases	GBenign

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Links from Gene

Items: 82