ClinVar Miner

List of variants in gene SERPINC1 reported as likely benign for secondary avascular necrosis

Included ClinVar conditions (7):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 101
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HGVS dbSNP gnomAD frequency
NM_000488.4(SERPINC1):c.89T>A (p.Val30Glu) rs2227624 0.00171
NM_000488.4(SERPINC1):c.1246G>T (p.Ala416Ser) rs121909548 0.00112
NM_000488.4(SERPINC1):c.218C>T (p.Pro73Leu) rs121909551 0.00092
NM_000488.4(SERPINC1):c.678C>T (p.Thr226=) rs2227627 0.00045
NM_000488.4(SERPINC1):c.529C>T (p.Arg177Cys) rs143521873 0.00041
NM_000488.4(SERPINC1):c.1005G>A (p.Val335=) rs192187532 0.00031
NM_000488.4(SERPINC1):c.-57G>A rs372524963 0.00029
NM_000488.4(SERPINC1):c.29C>A (p.Thr10Asn) rs61736655 0.00029
NM_000488.4(SERPINC1):c.870C>T (p.Phe290=) rs370190321 0.00026
NM_000488.4(SERPINC1):c.236G>A (p.Arg79His) rs121909552 0.00018
NM_000488.4(SERPINC1):c.910T>C (p.Leu304=) rs150507232 0.00015
NM_000488.4(SERPINC1):c.808C>T (p.Leu270=) rs139275128 0.00011
NM_000488.4(SERPINC1):c.299A>G (p.Asp100Gly) rs369524182 0.00009
NM_000488.4(SERPINC1):c.47T>C (p.Val16Ala) rs531137446 0.00008
NM_000488.4(SERPINC1):c.719A>G (p.Asn240Ser) rs200861147 0.00006
NM_000488.4(SERPINC1):c.1154-5T>C rs375346550 0.00005
NM_000488.4(SERPINC1):c.586T>C (p.Leu196=) rs781696456 0.00004
NM_000488.4(SERPINC1):c.708G>A (p.Ser236=) rs774632265 0.00004
NM_000488.4(SERPINC1):c.87C>T (p.Cys29=) rs188274879 0.00004
NM_000488.4(SERPINC1):c.1254C>T (p.Thr418=) rs559277597 0.00003
NM_000488.4(SERPINC1):c.594T>C (p.Tyr198=) rs183416252 0.00003
NM_000488.4(SERPINC1):c.99C>T (p.His33=) rs147676453 0.00003
NM_000488.4(SERPINC1):c.201C>T (p.Gly67=) rs773751914 0.00002
NM_000488.4(SERPINC1):c.219G>A (p.Pro73=) rs746429528 0.00002
NM_000488.4(SERPINC1):c.633A>G (p.Ala211=) rs780062808 0.00002
NM_000488.4(SERPINC1):c.1119C>T (p.Val373=) rs1271197978 0.00001
NM_000488.4(SERPINC1):c.1218+7A>G rs899914657 0.00001
NM_000488.4(SERPINC1):c.1278G>A (p.Ser426=) rs773792958 0.00001
NM_000488.4(SERPINC1):c.192G>A (p.Glu64=) rs1462236331 0.00001
NM_000488.4(SERPINC1):c.237T>C (p.Arg79=) rs781591817 0.00001
NM_000488.4(SERPINC1):c.408+4C>T rs201551398 0.00001
NM_000488.4(SERPINC1):c.468C>T (p.Ala156=) rs759369437 0.00001
NM_000488.4(SERPINC1):c.648G>A (p.Ala216=) rs767468032 0.00001
NM_000488.4(SERPINC1):c.756C>T (p.Tyr252=) rs745970800 0.00001
NM_000488.4(SERPINC1):c.881G>A (p.Arg294His) rs587776397 0.00001
NM_000488.4(SERPINC1):c.1008G>C (p.Leu336=)
NM_000488.4(SERPINC1):c.1020G>A (p.Leu340=)
NM_000488.4(SERPINC1):c.1047G>C (p.Val349=)
NM_000488.4(SERPINC1):c.105C>T (p.Ser35=)
NM_000488.4(SERPINC1):c.1077C>T (p.Asp359=)
NM_000488.4(SERPINC1):c.1107C>T (p.Asp369=)
NM_000488.4(SERPINC1):c.1153+7C>T
NM_000488.4(SERPINC1):c.1154-14G>C
NM_000488.4(SERPINC1):c.1154-15C>T
NM_000488.4(SERPINC1):c.1218+11C>T
NM_000488.4(SERPINC1):c.1219-16C>T
NM_000488.4(SERPINC1):c.1219-8A>G
NM_000488.4(SERPINC1):c.1242A>T (p.Ala414=)
NM_000488.4(SERPINC1):c.1275T>C (p.Arg425=) rs1227097057
NM_000488.4(SERPINC1):c.1284C>T (p.Asn428=)
NM_000488.4(SERPINC1):c.132G>A (p.Pro44=)
NM_000488.4(SERPINC1):c.1338A>G (p.Glu446=)
NM_000488.4(SERPINC1):c.1350C>T (p.Asn450=)
NM_000488.4(SERPINC1):c.1386T>C (p.Cys462=)
NM_000488.4(SERPINC1):c.138C>T (p.Asp46=)
NM_000488.4(SERPINC1):c.15G>T (p.Val5=)
NM_000488.4(SERPINC1):c.171C>T (p.Ser57=)
NM_000488.4(SERPINC1):c.174G>A (p.Pro58=)
NM_000488.4(SERPINC1):c.21A>T (p.Gly7=)
NM_000488.4(SERPINC1):c.240C>T (p.Val80=) rs2102789873
NM_000488.4(SERPINC1):c.30C>A (p.Thr10=)
NM_000488.4(SERPINC1):c.333A>G (p.Ser111=) rs2102789680
NM_000488.4(SERPINC1):c.337C>T (p.Leu113=)
NM_000488.4(SERPINC1):c.342T>C (p.Ser114=)
NM_000488.4(SERPINC1):c.345C>T (p.Ile115=)
NM_000488.4(SERPINC1):c.351G>A (p.Thr117=)
NM_000488.4(SERPINC1):c.366C>G (p.Thr122=) rs2102789624
NM_000488.4(SERPINC1):c.370C>T (p.Leu124=)
NM_000488.4(SERPINC1):c.409-11G>T
NM_000488.4(SERPINC1):c.409-8T>C
NM_000488.4(SERPINC1):c.41+12G>A
NM_000488.4(SERPINC1):c.417G>A (p.Lys139=) rs2102786232
NM_000488.4(SERPINC1):c.42-10C>A
NM_000488.4(SERPINC1):c.42-15T>C
NM_000488.4(SERPINC1):c.423C>T (p.Asp141=) rs1657792288
NM_000488.4(SERPINC1):c.495A>G (p.Lys165=)
NM_000488.4(SERPINC1):c.501C>T (p.Asn167=)
NM_000488.4(SERPINC1):c.51T>C (p.Tyr17=) rs2102790373
NM_000488.4(SERPINC1):c.525C>T (p.Ala175=) rs1553218235
NM_000488.4(SERPINC1):c.553A>G (p.Thr185Ala) rs574547491
NM_000488.4(SERPINC1):c.591A>G (p.Val197=)
NM_000488.4(SERPINC1):c.624+18C>T
NM_000488.4(SERPINC1):c.624+9C>T
NM_000488.4(SERPINC1):c.625-5C>G
NM_000488.4(SERPINC1):c.625-9T>C rs2102784825
NM_000488.4(SERPINC1):c.645A>G (p.Arg215=) rs863224366
NM_000488.4(SERPINC1):c.669C>A (p.Ser223=)
NM_000488.4(SERPINC1):c.678C>G (p.Thr226=)
NM_000488.4(SERPINC1):c.693C>A (p.Thr231=)
NM_000488.4(SERPINC1):c.705C>G (p.Pro235=)
NM_000488.4(SERPINC1):c.750C>A (p.Thr250=) rs1018454989
NM_000488.4(SERPINC1):c.762+19G>C
NM_000488.4(SERPINC1):c.762+7A>G rs2102784549
NM_000488.4(SERPINC1):c.777A>C (p.Ser259=) rs746961120
NM_000488.4(SERPINC1):c.834G>A (p.Ser278=)
NM_000488.4(SERPINC1):c.876T>C (p.Tyr292=)
NM_000488.4(SERPINC1):c.878G>A (p.Arg293Gln)
NM_000488.4(SERPINC1):c.882C>G (p.Arg294=) rs184508490
NM_000488.4(SERPINC1):c.882C>T (p.Arg294=)
NM_000488.4(SERPINC1):c.885G>T (p.Val295=)
NM_000488.4(SERPINC1):c.894C>T (p.Gly298=)

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