ClinVar Miner

List of variants in gene RNASEH2C reported as uncertain significance for Aicardi-Goutieres syndrome 3

Included ClinVar conditions (1):
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Total variants: 39
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HGVS dbSNP
NC_000011.10:g.65720897C>A
NC_000011.10:g.65720944T>G
NM_032193.3(RNASEH2C):c.*27C>G rs886048500
NM_032193.3(RNASEH2C):c.*29A>G rs886048499
NM_032193.3(RNASEH2C):c.-27G>T rs549471118
NM_032193.3(RNASEH2C):c.-89C>G rs886048503
NM_032193.3(RNASEH2C):c.115G>T (p.Asp39Tyr) rs773527127
NM_032193.3(RNASEH2C):c.169G>A (p.Glu57Lys) rs769127379
NM_032193.3(RNASEH2C):c.173-14G>A rs886048502
NM_032193.3(RNASEH2C):c.173-4C>G rs886048501
NM_032193.3(RNASEH2C):c.175C>A (p.Leu59Ile) rs764887792
NM_032193.3(RNASEH2C):c.260A>G (p.Glu87Gly) rs939276490
NM_032193.3(RNASEH2C):c.268A>G (p.Lys90Glu) rs200659526
NM_032193.3(RNASEH2C):c.268_269delinsGT (p.Lys90Val) rs1565213438
NM_032193.3(RNASEH2C):c.269A>T (p.Lys90Met) rs772347588
NM_032193.3(RNASEH2C):c.348+6C>T rs779293116
NM_032193.3(RNASEH2C):c.417C>G (p.Gly139=) rs147021687
NM_032193.3(RNASEH2C):c.434G>C (p.Arg145Pro) rs774773395
NM_032193.3(RNASEH2C):c.434G>T (p.Arg145Leu) rs774773395
NM_032193.3(RNASEH2C):c.468+5G>C rs753880827
NM_032193.3(RNASEH2C):c.468+8G>A rs751767695
NM_032193.3(RNASEH2C):c.472C>G (p.His158Asp) rs759118175
NM_032193.3(RNASEH2C):c.56C>G (p.Ala19Gly) rs773830258
NM_032193.4(RNASEH2C):c.*178C>G
NM_032193.4(RNASEH2C):c.*78A>G
NM_032193.4(RNASEH2C):c.115G>A (p.Asp39Asn)
NM_032193.4(RNASEH2C):c.142T>C (p.Phe48Leu)
NM_032193.4(RNASEH2C):c.235C>G (p.Leu79Val)
NM_032193.4(RNASEH2C):c.292C>T (p.Pro98Ser)
NM_032193.4(RNASEH2C):c.305C>T (p.Ser102Phe)
NM_032193.4(RNASEH2C):c.307G>A (p.Gly103Arg)
NM_032193.4(RNASEH2C):c.31A>G (p.Arg11Gly)
NM_032193.4(RNASEH2C):c.348C>G (p.Phe116Leu)
NM_032193.4(RNASEH2C):c.455G>A (p.Ser152Asn)
NM_032193.4(RNASEH2C):c.455G>T (p.Ser152Ile)
NM_032193.4(RNASEH2C):c.463G>A (p.Ala155Thr)
NM_032193.4(RNASEH2C):c.472C>T (p.His158Tyr)
NM_032193.4(RNASEH2C):c.49C>A (p.Arg17Ser)
NM_032193.4(RNASEH2C):c.59C>T (p.Thr20Ile)

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