Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.97549600T>ACA341377493DPYDc.1484A>T (p.Asp495Val)
c.1373A>T (p.Asp458Val)
c.989A>T (p.Asp330Val)
1g.97549600T>CCA27517937DPYDc.1484A>G (p.Asp495Gly)
c.1373A>G (p.Asp458Gly)
c.989A>G (p.Asp330Gly)
 dbSNP gnomAD v4
1g.97549600T>GCA341377495DPYDc.1484A>C (p.Asp495Ala)
c.1373A>C (p.Asp458Ala)
c.989A>C (p.Asp330Ala)
1g.97549600T=CA1141231464DPYDc.1484A= (p.Asp495=)
c.1373A= (p.Asp458=)
c.989A= (p.Asp330=)
1g.97549601C>ACA341377497DPYDc.1483G>T (p.Asp495Tyr)
c.1372G>T (p.Asp458Tyr)
c.988G>T (p.Asp330Tyr)
1g.97549601C=CA1182917400DPYDc.1483G= (p.Asp495=)
c.1372G= (p.Asp458=)
c.988G= (p.Asp330=)
1g.97549601C>GCA341377499DPYDc.1483G>C (p.Asp495His)
c.1372G>C (p.Asp458His)
c.988G>C (p.Asp330His)
1g.97549601C>TCA341377498DPYDc.1483G>A (p.Asp495Asn)
c.1372G>A (p.Asp458Asn)
c.988G>A (p.Asp330Asn)
 dbSNP COSMIC
1g.97549602A>CCA341377501DPYDc.1482T>G (p.Asn494Lys)
c.1371T>G (p.Asn457Lys)
c.987T>G (p.Asn329Lys)
1g.97549602A>GCA419145243DPYDc.1482T>C (p.Asn494=)
c.1371T>C (p.Asn457=)
c.987T>C (p.Asn329=)
1g.97549602A>TCA341377502DPYDc.1482T>A (p.Asn494Lys)
c.1371T>A (p.Asn457Lys)
c.987T>A (p.Asn329Lys)
1g.97549603T>ACA341377504DPYDc.1481A>T (p.Asn494Ile)
c.1370A>T (p.Asn457Ile)
c.986A>T (p.Asn329Ile)
1g.97549603T>CCA963338DPYDc.1481A>G (p.Asn494Ser)
c.1370A>G (p.Asn457Ser)
c.986A>G (p.Asn329Ser)
 dbSNP ExAC gnomAD v2 gnomAD v4
1g.97549603T>GCA341377506DPYDc.1481A>C (p.Asn494Thr)
c.1370A>C (p.Asn457Thr)
c.986A>C (p.Asn329Thr)
1g.97549603T=CA1182917401DPYDc.1481A= (p.Asn494=)
c.1370A= (p.Asn457=)
c.986A= (p.Asn329=)
1g.97549604T>ACA341377507DPYDc.1480A>T (p.Asn494Tyr)
c.1369A>T (p.Asn457Tyr)
c.985A>T (p.Asn329Tyr)
1g.97549604T>CCA341377509DPYDc.1480A>G (p.Asn494Asp)
c.1369A>G (p.Asn457Asp)
c.985A>G (p.Asn329Asp)
1g.97549604T>GCA341377511DPYDc.1480A>C (p.Asn494His)
c.1369A>C (p.Asn457His)
c.985A>C (p.Asn329His)
1g.97549605C>ACA419145247DPYDc.1479G>T (p.Val493=)
c.1368G>T (p.Val456=)
c.984G>T (p.Val328=)
1g.97549605C=CA1182917402DPYDc.1479G= (p.Val493=)
c.1368G= (p.Val456=)
c.984G= (p.Val328=)
1g.97549605C>GCA419145248DPYDc.1479G>C (p.Val493=)
c.1368G>C (p.Val456=)
c.984G>C (p.Val328=)
1g.97549605C>TCA419145249DPYDc.1479G>A (p.Val493=)
c.1368G>A (p.Val456=)
c.984G>A (p.Val328=)
 dbSNP gnomAD v2 gnomAD v4 COSMIC
1g.97549606A>CCA341377514DPYDc.1478T>G (p.Val493Gly)
c.1367T>G (p.Val456Gly)
c.983T>G (p.Val328Gly)
1g.97549606A>GCA341377516DPYDc.1478T>C (p.Val493Ala)
c.1367T>C (p.Val456Ala)
c.983T>C (p.Val328Ala)
 gnomAD v4
1g.97549606A>TCA341377518DPYDc.1478T>A (p.Val493Glu)
c.1367T>A (p.Val456Glu)
c.983T>A (p.Val328Glu)
1g.97549607C>ACA341377523DPYDc.1477G>T (p.Val493Leu)
c.1366G>T (p.Val456Leu)
c.982G>T (p.Val328Leu)
1g.97549607C=CA1182917403DPYDc.1477G= (p.Val493=)
c.1366G= (p.Val456=)
c.982G= (p.Val328=)
1g.97549607C>GCA341377531DPYDc.1477G>C (p.Val493Leu)
c.1366G>C (p.Val456Leu)
c.982G>C (p.Val328Leu)
1g.97549607C>TCA341377526DPYDc.1477G>A (p.Val493Met)
c.1366G>A (p.Val456Met)
c.982G>A (p.Val328Met)
 dbSNP gnomAD v2 gnomAD v4
1g.97549608C>ACA419145251DPYDc.1476G>T (p.Ser492=)
c.1365G>T (p.Ser455=)
c.981G>T (p.Ser327=)
1g.97549608C=CA1182917404DPYDc.1476G= (p.Ser492=)
c.1365G= (p.Ser455=)
c.981G= (p.Ser327=)
1g.97549608C>GCA419145253DPYDc.1476G>C (p.Ser492=)
c.1365G>C (p.Ser455=)
c.981G>C (p.Ser327=)
1g.97549608C>TCA963339DPYDc.1476G>A (p.Ser492=)
c.1365G>A (p.Ser455=)
c.981G>A (p.Ser327=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.97549609G>ACA963340DPYDc.1475C>T (p.Ser492Leu)
c.1364C>T (p.Ser455Leu)
c.980C>T (p.Ser327Leu)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
1g.97549609G>CCA341377534DPYDc.1475C>G (p.Ser492Trp)
c.1364C>G (p.Ser455Trp)
c.980C>G (p.Ser327Trp)
 dbSNP gnomAD v2 gnomAD v4
1g.97549609G=CA1140803050DPYDc.1475C= (p.Ser492=)
c.1364C= (p.Ser455=)
c.980C= (p.Ser327=)
1g.97549609G>TCA341377536DPYDc.1475C>A (p.Ser492Ter)
c.1364C>A (p.Ser455Ter)
c.980C>A (p.Ser327Ter)
 dbSNP gnomAD v2 gnomAD v4
1g.97549610A>CCA341377538DPYDc.1474T>G (p.Ser492Ala)
c.1363T>G (p.Ser455Ala)
c.979T>G (p.Ser327Ala)
 gnomAD v4
1g.97549610A>GCA341377540DPYDc.1474T>C (p.Ser492Pro)
c.1363T>C (p.Ser455Pro)
c.979T>C (p.Ser327Pro)
1g.97549610A>TCA341377542DPYDc.1474T>A (p.Ser492Thr)
c.1363T>A (p.Ser455Thr)
c.979T>A (p.Ser327Thr)
1g.97549611T>ACA341377543DPYDc.1473A>T (p.Glu491Asp)
c.1362A>T (p.Glu454Asp)
c.978A>T (p.Glu326Asp)
1g.97549611T>CCA419145255DPYDc.1473A>G (p.Glu491=)
c.1362A>G (p.Glu454=)
c.978A>G (p.Glu326=)
 dbSNP
1g.97549611T>GCA27517953DPYDc.1473A>C (p.Glu491Asp)
c.1362A>C (p.Glu454Asp)
c.978A>C (p.Glu326Asp)
 dbSNP gnomAD v3 gnomAD v4
1g.97549611T=CA1182917405DPYDc.1473A= (p.Glu491=)
c.1362A= (p.Glu454=)
c.978A= (p.Glu326=)
1g.97549612T>ACA341377544DPYDc.1472A>T (p.Glu491Val)
c.1361A>T (p.Glu454Val)
c.977A>T (p.Glu326Val)
 dbSNP gnomAD v3 gnomAD v4
1g.97549612T>CCA341377545DPYDc.1472A>G (p.Glu491Gly)
c.1361A>G (p.Glu454Gly)
c.977A>G (p.Glu326Gly)
 gnomAD v4
1g.97549612T>GCA341377547DPYDc.1472A>C (p.Glu491Ala)
c.1361A>C (p.Glu454Ala)
c.977A>C (p.Glu326Ala)
1g.97549612T=CA1182917406DPYDc.1472A= (p.Glu491=)
c.1361A= (p.Glu454=)
c.977A= (p.Glu326=)
1g.97549613C>ACA341377550DPYDc.1471G>T (p.Glu491Ter)
c.1360G>T (p.Glu454Ter)
c.976G>T (p.Glu326Ter)
1g.97549613C>GCA341377551DPYDc.1471G>C (p.Glu491Gln)
c.1360G>C (p.Glu454Gln)
c.976G>C (p.Glu326Gln)

Number of alleles fetched