Related gene-specific medical variations for Gene (Select 246243) - ClinVar - NCBI

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Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3000562	NM_002936.6(RNASEH1):c.40G>A (p.Ala14Thr)	LOC129933002, RNASEH1 (A14T)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 2838843	NM_002936.6(RNASEH1):c.42C>A (p.Ala14=)	LOC129933002, RNASEH1	Single nucleotide variant (5 prime UTR variant +2 more)	not provided	GLikely benign
Select item 2830192	NM_002936.6(RNASEH1):c.15G>C (p.Leu5=)	LOC129933002, RNASEH1	Single nucleotide variant (5 prime UTR variant +2 more)	not provided	GLikely benign
Select item 2474680	NM_002936.6(RNASEH1):c.65C>G (p.Ser22Cys)	LOC129933002, RNASEH1 (S22C)	Single nucleotide variant (5 prime UTR variant +2 more)	Inborn genetic diseases	GLikely benign
Select item 2236836	NM_002936.6(RNASEH1):c.25C>T (p.His9Tyr)	LOC129933002, RNASEH1 (H9Y)	Single nucleotide variant (5 prime UTR variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2167915	NM_002936.6(RNASEH1):c.65C>T (p.Ser22Phe)	LOC129933002, RNASEH1 (S22F)	Single nucleotide variant (5 prime UTR variant +2 more)	not provided +1 more	GUncertain significance
Select item 2142955	NM_002936.6(RNASEH1):c.68G>A (p.Arg23His)	LOC129933002, RNASEH1 (R23H)	Single nucleotide variant (5 prime UTR variant +2 more)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2084621	NM_002936.6(RNASEH1):c.5G>C (p.Ser2Thr)	LOC129933002, RNASEH1 (S2T)	Single nucleotide variant (5 prime UTR variant +2 more)	not provided	GUncertain significance
Select item 2071909	NM_002936.6(RNASEH1):c.72G>T (p.Gly24=)	LOC129933002, RNASEH1	Single nucleotide variant (5 prime UTR variant +2 more)	not provided	GLikely benign
Select item 1911823	NM_002936.6(RNASEH1):c.57C>T (p.Arg19=)	LOC129933002, RNASEH1	Single nucleotide variant (5 prime UTR variant +2 more)	not provided	GLikely benign
Select item 1901426	NM_002936.6(RNASEH1):c.15G>T (p.Leu5=)	LOC129933002, RNASEH1	Single nucleotide variant (5 prime UTR variant +2 more)	not provided	GLikely benign
Select item 1706193	NM_002936.6(RNASEH1):c.58C>T (p.Arg20Cys)	LOC129933002, RNASEH1 (R20C)	Single nucleotide variant (5 prime UTR variant +2 more)	Inborn genetic diseases +1 more	GConflicting classifications of pathogenicity
Select item 1275935	NM_002936.6(RNASEH1):c.-56G>T	LOC129933002, RNASEH1	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GBenign
Select item 1212161	NM_002936.6(RNASEH1):c.-47C>T	RNASEH1, LOC129933002	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GLikely benign
Select item 741378	NM_002936.6(RNASEH1):c.51C>T (p.Pro17=)	LOC129933002, RNASEH1	Single nucleotide variant (5 prime UTR variant +2 more)	not provided	GLikely benign