Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.68885629T>ACA470274099STOX1c.1833T>A (p.Gly611=)
c.2169T>A (p.Gly723=)
c.463+3519T>A (n.463+3519T>A)
c.663+1170T>A (n.663+1170T>A)
c.1503T>A (p.Gly501=)
10g.68885629T>CCA470274101STOX1c.1833T>C (p.Gly611=)
c.2169T>C (p.Gly723=)
c.463+3519T>C (n.463+3519T>C)
c.663+1170T>C (n.663+1170T>C)
c.1503T>C (p.Gly501=)
10g.68885629T>GCA470274100STOX1c.1833T>G (p.Gly611=)
c.2169T>G (p.Gly723=)
c.463+3519T>G (n.463+3519T>G)
c.663+1170T>G (n.663+1170T>G)
c.1503T>G (p.Gly501=)
10g.68885630G>ACA376881933STOX1c.1834G>A (p.Gly612Arg)
c.2170G>A (p.Gly724Arg)
c.463+3520G>A (n.463+3520G>A)
c.663+1171G>A (n.663+1171G>A)
c.1504G>A (p.Gly502Arg)
10g.68885630G>CCA376881934STOX1c.1834G>C (p.Gly612Arg)
c.2170G>C (p.Gly724Arg)
c.463+3520G>C (n.463+3520G>C)
c.663+1171G>C (n.663+1171G>C)
c.1504G>C (p.Gly502Arg)
10g.68885630G>TCA376881935STOX1c.1834G>T (p.Gly612Ter)
c.2170G>T (p.Gly724Ter)
c.463+3520G>T (n.463+3520G>T)
c.663+1171G>T (n.663+1171G>T)
c.1504G>T (p.Gly502Ter)
10g.68885631G>ACA208268314STOX1c.1835G>A (p.Gly612Glu)
c.2171G>A (p.Gly724Glu)
c.463+3521G>A (n.463+3521G>A)
c.663+1172G>A (n.663+1172G>A)
c.1505G>A (p.Gly502Glu)
dbSNP
10g.68885631G>CCA376881936STOX1c.1835G>C (p.Gly612Ala)
c.2171G>C (p.Gly724Ala)
c.463+3521G>C (n.463+3521G>C)
c.663+1172G>C (n.663+1172G>C)
c.1505G>C (p.Gly502Ala)
10g.68885631G=CA1917550064STOX1c.1835G= (p.Gly612=)
c.2171G= (p.Gly724=)
c.463+3521G= (n.463+3521G=)
c.663+1172G= (n.663+1172G=)
c.1505G= (p.Gly502=)
10g.68885631G>TCA376881937STOX1c.1835G>T (p.Gly612Val)
c.2171G>T (p.Gly724Val)
c.463+3521G>T (n.463+3521G>T)
c.663+1172G>T (n.663+1172G>T)
c.1505G>T (p.Gly502Val)
10g.68885632A>CCA470274102STOX1c.1836A>C (p.Gly612=)
c.2172A>C (p.Gly724=)
c.463+3522A>C (n.463+3522A>C)
c.663+1173A>C (n.663+1173A>C)
c.1506A>C (p.Gly502=)
10g.68885632A>GCA470274103STOX1c.1836A>G (p.Gly612=)
c.2172A>G (p.Gly724=)
c.463+3522A>G (n.463+3522A>G)
c.663+1173A>G (n.663+1173A>G)
c.1506A>G (p.Gly502=)
10g.68885632A>TCA470274104STOX1c.1836A>T (p.Gly612=)
c.2172A>T (p.Gly724=)
c.463+3522A>T (n.463+3522A>T)
c.663+1173A>T (n.663+1173A>T)
c.1506A>T (p.Gly502=)
10g.68885633G>ACA376881938STOX1c.1837G>A (p.Glu613Lys)
c.2173G>A (p.Glu725Lys)
c.463+3523G>A (n.463+3523G>A)
c.663+1174G>A (n.663+1174G>A)
c.1507G>A (p.Glu503Lys)
10g.68885633G>CCA376881939STOX1c.1837G>C (p.Glu613Gln)
c.2173G>C (p.Glu725Gln)
c.463+3523G>C (n.463+3523G>C)
c.663+1174G>C (n.663+1174G>C)
c.1507G>C (p.Glu503Gln)
gnomAD v4
10g.68885633G>TCA376881940STOX1c.1837G>T (p.Glu613Ter)
c.2173G>T (p.Glu725Ter)
c.463+3523G>T (n.463+3523G>T)
c.663+1174G>T (n.663+1174G>T)
c.1507G>T (p.Glu503Ter)
10g.68885634A>CCA376881943STOX1c.1838A>C (p.Glu613Ala)
c.2174A>C (p.Glu725Ala)
c.463+3524A>C (n.463+3524A>C)
c.663+1175A>C (n.663+1175A>C)
c.1508A>C (p.Glu503Ala)
10g.68885634A>GCA376881941STOX1c.1838A>G (p.Glu613Gly)
c.2174A>G (p.Glu725Gly)
c.463+3524A>G (n.463+3524A>G)
c.663+1175A>G (n.663+1175A>G)
c.1508A>G (p.Glu503Gly)
10g.68885634A>TCA376881942STOX1c.1838A>T (p.Glu613Val)
c.2174A>T (p.Glu725Val)
c.463+3524A>T (n.463+3524A>T)
c.663+1175A>T (n.663+1175A>T)
c.1508A>T (p.Glu503Val)
10g.68885637delCA470274105STOX1c.1841del (p.Asn614MetfsTer3)
c.2177del (p.Asn726MetfsTer3)
c.463+3527del (n.463+3527del)
c.663+1178del (n.663+1178del)
c.1511del (p.Asn504MetfsTer3)
COSMIC
10g.68885635A>CCA376881944STOX1c.1839A>C (p.Glu613Asp)
c.2175A>C (p.Glu725Asp)
c.463+3525A>C (n.463+3525A>C)
c.663+1176A>C (n.663+1176A>C)
c.1509A>C (p.Glu503Asp)
10g.68885635A>GCA470274106STOX1c.1839A>G (p.Glu613=)
c.2175A>G (p.Glu725=)
c.463+3525A>G (n.463+3525A>G)
c.663+1176A>G (n.663+1176A>G)
c.1509A>G (p.Glu503=)
10g.68885635A>TCA376881945STOX1c.1839A>T (p.Glu613Asp)
c.2175A>T (p.Glu725Asp)
c.463+3525A>T (n.463+3525A>T)
c.663+1176A>T (n.663+1176A>T)
c.1509A>T (p.Glu503Asp)
10g.68885636A>CCA376881946STOX1c.1840A>C (p.Asn614His)
c.2176A>C (p.Asn726His)
c.463+3526A>C (n.463+3526A>C)
c.663+1177A>C (n.663+1177A>C)
c.1510A>C (p.Asn504His)
10g.68885636A>GCA376881947STOX1c.1840A>G (p.Asn614Asp)
c.2176A>G (p.Asn726Asp)
c.463+3526A>G (n.463+3526A>G)
c.663+1177A>G (n.663+1177A>G)
c.1510A>G (p.Asn504Asp)
10g.68885636A>TCA376881948STOX1c.1840A>T (p.Asn614Tyr)
c.2176A>T (p.Asn726Tyr)
c.463+3526A>T (n.463+3526A>T)
c.663+1177A>T (n.663+1177A>T)
c.1510A>T (p.Asn504Tyr)
10g.68885637A>CCA376881949STOX1c.1841A>C (p.Asn614Thr)
c.2177A>C (p.Asn726Thr)
c.463+3527A>C (n.463+3527A>C)
c.663+1178A>C (n.663+1178A>C)
c.1511A>C (p.Asn504Thr)
gnomAD v4
10g.68885637A>GCA376881950STOX1c.1841A>G (p.Asn614Ser)
c.2177A>G (p.Asn726Ser)
c.463+3527A>G (n.463+3527A>G)
c.663+1178A>G (n.663+1178A>G)
c.1511A>G (p.Asn504Ser)
10g.68885637A>TCA376881951STOX1c.1841A>T (p.Asn614Ile)
c.2177A>T (p.Asn726Ile)
c.463+3527A>T (n.463+3527A>T)
c.663+1178A>T (n.663+1178A>T)
c.1511A>T (p.Asn504Ile)
10g.68885638T>ACA376881952STOX1c.1842T>A (p.Asn614Lys)
c.2178T>A (p.Asn726Lys)
c.463+3528T>A (n.463+3528T>A)
c.663+1179T>A (n.663+1179T>A)
c.1512T>A (p.Asn504Lys)
10g.68885638T>CCA470274107STOX1c.1842T>C (p.Asn614=)
c.2178T>C (p.Asn726=)
c.463+3528T>C (n.463+3528T>C)
c.663+1179T>C (n.663+1179T>C)
c.1512T>C (p.Asn504=)
10g.68885638T>GCA376881953STOX1c.1842T>G (p.Asn614Lys)
c.2178T>G (p.Asn726Lys)
c.463+3528T>G (n.463+3528T>G)
c.663+1179T>G (n.663+1179T>G)
c.1512T>G (p.Asn504Lys)
dbSNP
10g.68885638T=CA1917550065STOX1c.1842T= (p.Asn614=)
c.2178T= (p.Asn726=)
c.463+3528T= (n.463+3528T=)
c.663+1179T= (n.663+1179T=)
c.1512T= (p.Asn504=)
10g.68885639G>ACA376881954STOX1c.1843G>A (p.Glu615Lys)
c.2179G>A (p.Glu727Lys)
c.463+3529G>A (n.463+3529G>A)
c.663+1180G>A (n.663+1180G>A)
c.1513G>A (p.Glu505Lys)
dbSNP gnomAD v3 gnomAD v4
10g.68885639G>CCA376881955STOX1c.1843G>C (p.Glu615Gln)
c.2179G>C (p.Glu727Gln)
c.463+3529G>C (n.463+3529G>C)
c.663+1180G>C (n.663+1180G>C)
c.1513G>C (p.Glu505Gln)
10g.68885639G=CA1917550066STOX1c.1843G= (p.Glu615=)
c.2179G= (p.Glu727=)
c.463+3529G= (n.463+3529G=)
c.663+1180G= (n.663+1180G=)
c.1513G= (p.Glu505=)
10g.68885639G>TCA376881956STOX1c.1843G>T (p.Glu615Ter)
c.2179G>T (p.Glu727Ter)
c.463+3529G>T (n.463+3529G>T)
c.663+1180G>T (n.663+1180G>T)
c.1513G>T (p.Glu505Ter)
10g.68885640A>CCA376881959STOX1c.1844A>C (p.Glu615Ala)
c.2180A>C (p.Glu727Ala)
c.463+3530A>C (n.463+3530A>C)
c.663+1181A>C (n.663+1181A>C)
c.1514A>C (p.Glu505Ala)
10g.68885640A>GCA376881958STOX1c.1844A>G (p.Glu615Gly)
c.2180A>G (p.Glu727Gly)
c.463+3530A>G (n.463+3530A>G)
c.663+1181A>G (n.663+1181A>G)
c.1514A>G (p.Glu505Gly)
10g.68885640A>TCA376881957STOX1c.1844A>T (p.Glu615Val)
c.2180A>T (p.Glu727Val)
c.463+3530A>T (n.463+3530A>T)
c.663+1181A>T (n.663+1181A>T)
c.1514A>T (p.Glu505Val)
10g.68885641G>ACA5528237STOX1c.1845G>A (p.Glu615=)
c.2181G>A (p.Glu727=)
c.463+3531G>A (n.463+3531G>A)
c.663+1182G>A (n.663+1182G>A)
c.1515G>A (p.Glu505=)
dbSNP ExAC gnomAD v2 gnomAD v4
10g.68885641G>CCA376881960STOX1c.1845G>C (p.Glu615Asp)
c.2181G>C (p.Glu727Asp)
c.463+3531G>C (n.463+3531G>C)
c.663+1182G>C (n.663+1182G>C)
c.1515G>C (p.Glu505Asp)
10g.68885641G=CA1917550067STOX1c.1845G= (p.Glu615=)
c.2181G= (p.Glu727=)
c.463+3531G= (n.463+3531G=)
c.663+1182G= (n.663+1182G=)
c.1515G= (p.Glu505=)
10g.68885641G>TCA376881961STOX1c.1845G>T (p.Glu615Asp)
c.2181G>T (p.Glu727Asp)
c.463+3531G>T (n.463+3531G>T)
c.663+1182G>T (n.663+1182G>T)
c.1515G>T (p.Glu505Asp)
dbSNP gnomAD v2 gnomAD v4
10g.68885642G>ACA376881962STOX1c.1846G>A (p.Val616Ile)
c.2182G>A (p.Val728Ile)
c.463+3532G>A (n.463+3532G>A)
c.663+1183G>A (n.663+1183G>A)
c.1516G>A (p.Val506Ile)
10g.68885642G>CCA376881963STOX1c.1846G>C (p.Val616Leu)
c.2182G>C (p.Val728Leu)
c.463+3532G>C (n.463+3532G>C)
c.663+1183G>C (n.663+1183G>C)
c.1516G>C (p.Val506Leu)
dbSNP
10g.68885642G=CA1917550068STOX1c.1846G= (p.Val616=)
c.2182G= (p.Val728=)
c.463+3532G= (n.463+3532G=)
c.663+1183G= (n.663+1183G=)
c.1516G= (p.Val506=)
10g.68885642G>TCA376881964STOX1c.1846G>T (p.Val616Leu)
c.2182G>T (p.Val728Leu)
c.463+3532G>T (n.463+3532G>T)
c.663+1183G>T (n.663+1183G>T)
c.1516G>T (p.Val506Leu)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.68885643T>ACA376881965STOX1c.1847T>A (p.Val616Glu)
c.2183T>A (p.Val728Glu)
c.463+3533T>A (n.463+3533T>A)
c.663+1184T>A (n.663+1184T>A)
c.1517T>A (p.Val506Glu)
10g.68885643T>CCA208268325STOX1c.1847T>C (p.Val616Ala)
c.2183T>C (p.Val728Ala)
c.463+3533T>C (n.463+3533T>C)
c.663+1184T>C (n.663+1184T>C)
c.1517T>C (p.Val506Ala)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4

Number of alleles fetched