Chr Mutation (hg38) CAid Gene Transcript Linkouts
Yg.12833700A>CCA414998651USP9Yc.5034A>C (p.Glu1678Asp)
n.5046A>C
c.4800A>C (p.Glu1600Asp)
c.5049A>C (p.Glu1683Asp)
Yg.12833700A>GCA519901463USP9Yc.5034A>G (p.Glu1678=)
n.5046A>G
c.4800A>G (p.Glu1600=)
c.5049A>G (p.Glu1683=)
Yg.12833700A>TCA414998650USP9Yc.5034A>T (p.Glu1678Asp)
n.5046A>T
c.4800A>T (p.Glu1600Asp)
c.5049A>T (p.Glu1683Asp)
Yg.12833701C>ACA414998653USP9Yc.5035C>A (p.Pro1679Thr)
n.5047C>A
c.4801C>A (p.Pro1601Thr)
c.5050C>A (p.Pro1684Thr)
Yg.12833701C>GCA414998655USP9Yc.5035C>G (p.Pro1679Ala)
n.5047C>G
c.4801C>G (p.Pro1601Ala)
c.5050C>G (p.Pro1684Ala)
Yg.12833701C>TCA414998657USP9Yc.5035C>T (p.Pro1679Ser)
n.5047C>T
c.4801C>T (p.Pro1601Ser)
c.5050C>T (p.Pro1684Ser)
Yg.12833702C>ACA337720909USP9Yc.5036C>A (p.Pro1679His)
n.5048C>A
c.4802C>A (p.Pro1601His)
c.5051C>A (p.Pro1684His)
dbSNP
Yg.12833702C=CA2470560445USP9Yc.5036C= (p.Pro1679=)
n.5048C=
c.4802C= (p.Pro1601=)
c.5051C= (p.Pro1684=)
Yg.12833702C>GCA414998660USP9Yc.5036C>G (p.Pro1679Arg)
n.5048C>G
c.4802C>G (p.Pro1601Arg)
c.5051C>G (p.Pro1684Arg)
Yg.12833702C>TCA414998662USP9Yc.5036C>T (p.Pro1679Leu)
n.5048C>T
c.4802C>T (p.Pro1601Leu)
c.5051C>T (p.Pro1684Leu)
Yg.12833703T>ACA519901471USP9Yc.5037T>A (p.Pro1679=)
n.5049T>A
c.4803T>A (p.Pro1601=)
c.5052T>A (p.Pro1684=)
Yg.12833703T>CCA519901474USP9Yc.5037T>C (p.Pro1679=)
n.5049T>C
c.4803T>C (p.Pro1601=)
c.5052T>C (p.Pro1684=)
Yg.12833703T>GCA519901475USP9Yc.5037T>G (p.Pro1679=)
n.5049T>G
c.4803T>G (p.Pro1601=)
c.5052T>G (p.Pro1684=)
Yg.12833704G>ACA414998665USP9Yc.5038G>A (p.Val1680Ile)
n.5050G>A
c.4804G>A (p.Val1602Ile)
c.5053G>A (p.Val1685Ile)
Yg.12833704G>CCA414998668USP9Yc.5038G>C (p.Val1680Leu)
n.5050G>C
c.4804G>C (p.Val1602Leu)
c.5053G>C (p.Val1685Leu)
Yg.12833704G>TCA414998666USP9Yc.5038G>T (p.Val1680Phe)
n.5050G>T
c.4804G>T (p.Val1602Phe)
c.5053G>T (p.Val1685Phe)
Yg.12833705T>ACA414998670USP9Yc.5039T>A (p.Val1680Asp)
n.5051T>A
c.4805T>A (p.Val1602Asp)
c.5054T>A (p.Val1685Asp)
Yg.12833705T>CCA414998671USP9Yc.5039T>C (p.Val1680Ala)
n.5051T>C
c.4805T>C (p.Val1602Ala)
c.5054T>C (p.Val1685Ala)
Yg.12833705T>GCA414998673USP9Yc.5039T>G (p.Val1680Gly)
n.5051T>G
c.4805T>G (p.Val1602Gly)
c.5054T>G (p.Val1685Gly)
Yg.12833706T>ACA519901486USP9Yc.5040T>A (p.Val1680=)
n.5052T>A
c.4806T>A (p.Val1602=)
c.5055T>A (p.Val1685=)
Yg.12833706T>CCA519901484USP9Yc.5040T>C (p.Val1680=)
n.5052T>C
c.4806T>C (p.Val1602=)
c.5055T>C (p.Val1685=)
Yg.12833706T>GCA519901482USP9Yc.5040T>G (p.Val1680=)
n.5052T>G
c.4806T>G (p.Val1602=)
c.5055T>G (p.Val1685=)
Yg.12833707A>CCA414998675USP9Yc.5041A>C (p.Asn1681His)
n.5053A>C
c.4807A>C (p.Asn1603His)
c.5056A>C (p.Asn1686His)
Yg.12833707A>GCA414998677USP9Yc.5041A>G (p.Asn1681Asp)
n.5053A>G
c.4807A>G (p.Asn1603Asp)
c.5056A>G (p.Asn1686Asp)
Yg.12833707A>TCA414998678USP9Yc.5041A>T (p.Asn1681Tyr)
n.5053A>T
c.4807A>T (p.Asn1603Tyr)
c.5056A>T (p.Asn1686Tyr)
Yg.12833708A>CCA414998681USP9Yc.5042A>C (p.Asn1681Thr)
n.5054A>C
c.4808A>C (p.Asn1603Thr)
c.5057A>C (p.Asn1686Thr)
Yg.12833708A>GCA414998682USP9Yc.5042A>G (p.Asn1681Ser)
n.5054A>G
c.4808A>G (p.Asn1603Ser)
c.5057A>G (p.Asn1686Ser)
Yg.12833708A>TCA414998684USP9Yc.5042A>T (p.Asn1681Ile)
n.5054A>T
c.4808A>T (p.Asn1603Ile)
c.5057A>T (p.Asn1686Ile)
Yg.12833709T>ACA414998686USP9Yc.5043T>A (p.Asn1681Lys)
n.5055T>A
c.4809T>A (p.Asn1603Lys)
c.5058T>A (p.Asn1686Lys)
Yg.12833709T>CCA519901494USP9Yc.5043T>C (p.Asn1681=)
n.5055T>C
c.4809T>C (p.Asn1603=)
c.5058T>C (p.Asn1686=)
Yg.12833709T>GCA414998688USP9Yc.5043T>G (p.Asn1681Lys)
n.5055T>G
c.4809T>G (p.Asn1603Lys)
c.5058T>G (p.Asn1686Lys)
Yg.12833710C>ACA414998689USP9Yc.5044C>A (p.Leu1682Ile)
n.5056C>A
c.4810C>A (p.Leu1604Ile)
c.5059C>A (p.Leu1687Ile)
Yg.12833710C>GCA414998694USP9Yc.5044C>G (p.Leu1682Val)
n.5056C>G
c.4810C>G (p.Leu1604Val)
c.5059C>G (p.Leu1687Val)
Yg.12833710C>TCA414998692USP9Yc.5044C>T (p.Leu1682Phe)
n.5056C>T
c.4810C>T (p.Leu1604Phe)
c.5059C>T (p.Leu1687Phe)
Yg.12833711T>ACA414998696USP9Yc.5045T>A (p.Leu1682His)
n.5057T>A
c.4811T>A (p.Leu1604His)
c.5060T>A (p.Leu1687His)
Yg.12833711T>CCA414998698USP9Yc.5045T>C (p.Leu1682Pro)
n.5057T>C
c.4811T>C (p.Leu1604Pro)
c.5060T>C (p.Leu1687Pro)
Yg.12833711T>GCA414998700USP9Yc.5045T>G (p.Leu1682Arg)
n.5057T>G
c.4811T>G (p.Leu1604Arg)
c.5060T>G (p.Leu1687Arg)
Yg.12833712C>ACA519901503USP9Yc.5046C>A (p.Leu1682=)
n.5058C>A
c.4812C>A (p.Leu1604=)
c.5061C>A (p.Leu1687=)
Yg.12833712C>GCA519901507USP9Yc.5046C>G (p.Leu1682=)
n.5058C>G
c.4812C>G (p.Leu1604=)
c.5061C>G (p.Leu1687=)
Yg.12833712C>TCA519901505USP9Yc.5046C>T (p.Leu1682=)
n.5058C>T
c.4812C>T (p.Leu1604=)
c.5061C>T (p.Leu1687=)
Yg.12833713C>ACA414998703USP9Yc.5047C>A (p.Arg1683Ser)
n.5059C>A
c.4813C>A (p.Arg1605Ser)
c.5062C>A (p.Arg1688Ser)
Yg.12833713C=CA2470560446USP9Yc.5047C= (p.Arg1683=)
n.5059C=
c.4813C= (p.Arg1605=)
c.5062C= (p.Arg1688=)
Yg.12833713C>GCA414998705USP9Yc.5047C>G (p.Arg1683Gly)
n.5059C>G
c.4813C>G (p.Arg1605Gly)
c.5062C>G (p.Arg1688Gly)
Yg.12833713C>TCA414998707USP9Yc.5047C>T (p.Arg1683Cys)
n.5059C>T
c.4813C>T (p.Arg1605Cys)
c.5062C>T (p.Arg1688Cys)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
Yg.12833714G>ACA10573378USP9Yc.5048G>A (p.Arg1683His)
n.5060G>A
c.4814G>A (p.Arg1605His)
c.5063G>A (p.Arg1688His)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Yg.12833714G>CCA414998710USP9Yc.5048G>C (p.Arg1683Pro)
n.5060G>C
c.4814G>C (p.Arg1605Pro)
c.5063G>C (p.Arg1688Pro)
Yg.12833714G=CA2470560447USP9Yc.5048G= (p.Arg1683=)
n.5060G=
c.4814G= (p.Arg1605=)
c.5063G= (p.Arg1688=)
Yg.12833714G>TCA414998712USP9Yc.5048G>T (p.Arg1683Leu)
n.5060G>T
c.4814G>T (p.Arg1605Leu)
c.5063G>T (p.Arg1688Leu)
Yg.12833715T>ACA519901515USP9Yc.5049T>A (p.Arg1683=)
n.5061T>A
c.4815T>A (p.Arg1605=)
c.5064T>A (p.Arg1688=)
Yg.12833715T>CCA519901517USP9Yc.5049T>C (p.Arg1683=)
n.5061T>C
c.4815T>C (p.Arg1605=)
c.5064T>C (p.Arg1688=)

Number of alleles fetched