ClinVar Miner

List of variants in gene SHOC2 reported as likely benign for not specified

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Total variants: 26
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HGVS dbSNP gnomAD frequency
NM_007373.4(SHOC2):c.1302C>T (p.Asn434=) rs146147503 0.00262
NM_007373.4(SHOC2):c.-179T>A rs143180451 0.00080
NM_007373.4(SHOC2):c.1162-16T>G rs376859485 0.00052
NM_007373.4(SHOC2):c.704-16G>T rs185614302 0.00033
NM_007373.4(SHOC2):c.841+12G>A rs201258692 0.00019
NM_007373.4(SHOC2):c.377C>T (p.Thr126Ile) rs138375593 0.00011
NM_007373.4(SHOC2):c.1161+9A>G rs201795589 0.00008
NM_007373.4(SHOC2):c.1239G>T (p.Gln413His) rs200215822 0.00006
NM_007373.4(SHOC2):c.610A>G (p.Ile204Val) rs200015085 0.00006
NM_007373.4(SHOC2):c.10A>C (p.Ser4Arg) rs397517231 0.00004
NM_007373.4(SHOC2):c.1541-10T>G rs202207809 0.00004
NM_007373.4(SHOC2):c.1731A>G (p.Pro577=) rs370929606 0.00004
NM_007373.4(SHOC2):c.170C>T (p.Ser57Phe) rs536611911 0.00003
NM_007373.4(SHOC2):c.-125C>T rs188765124 0.00002
NM_007373.4(SHOC2):c.1337A>G (p.Asn446Ser) rs730881017 0.00002
NM_007373.4(SHOC2):c.171C>T (p.Ser57=) rs1554857645 0.00001
NM_007373.4(SHOC2):c.303T>C (p.Asn101=) rs750568201 0.00001
NM_007373.4(SHOC2):c.333T>C (p.Ser111=) rs758161464 0.00001
NM_007373.4(SHOC2):c.842-3C>T rs1485718634 0.00001
NM_007373.4(SHOC2):c.-234-14A>G rs1554857573
NM_007373.4(SHOC2):c.-66A>G rs397517230
NM_007373.4(SHOC2):c.1335A>G (p.Gly445=)
NM_007373.4(SHOC2):c.1481C>A (p.Thr494Asn) rs758241851
NM_007373.4(SHOC2):c.567T>C (p.Tyr189=) rs1847644303
NM_007373.4(SHOC2):c.96A>T (p.Gly32=) rs1847633735
NM_007373.4(SHOC2):c.973-5del rs730881016

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