Chr Mutation (hg38) CAid Gene Transcript Linkouts
Yg.12833691T>ACA519901429USP9Yc.5025T>A (p.Leu1675=)
n.5037T>A
c.4791T>A (p.Leu1597=)
c.5040T>A (p.Leu1680=)
Yg.12833691T>CCA519901431USP9Yc.5025T>C (p.Leu1675=)
n.5037T>C
c.4791T>C (p.Leu1597=)
c.5040T>C (p.Leu1680=)
Yg.12833691T>GCA519901432USP9Yc.5025T>G (p.Leu1675=)
n.5037T>G
c.4791T>G (p.Leu1597=)
c.5040T>G (p.Leu1680=)
Yg.12833692T>ACA414998611USP9Yc.5026T>A (p.Trp1676Arg)
n.5038T>A
c.4792T>A (p.Trp1598Arg)
c.5041T>A (p.Trp1681Arg)
Yg.12833692T>CCA414998612USP9Yc.5026T>C (p.Trp1676Arg)
n.5038T>C
c.4792T>C (p.Trp1598Arg)
c.5041T>C (p.Trp1681Arg)
Yg.12833692T>GCA414998614USP9Yc.5026T>G (p.Trp1676Gly)
n.5038T>G
c.4792T>G (p.Trp1598Gly)
c.5041T>G (p.Trp1681Gly)
Yg.12833693G>ACA414998617USP9Yc.5027G>A (p.Trp1676Ter)
n.5039G>A
c.4793G>A (p.Trp1598Ter)
c.5042G>A (p.Trp1681Ter)
Yg.12833693G>CCA414998618USP9Yc.5027G>C (p.Trp1676Ser)
n.5039G>C
c.4793G>C (p.Trp1598Ser)
c.5042G>C (p.Trp1681Ser)
Yg.12833693G>TCA414998619USP9Yc.5027G>T (p.Trp1676Leu)
n.5039G>T
c.4793G>T (p.Trp1598Leu)
c.5042G>T (p.Trp1681Leu)
Yg.12833694G>ACA414998621USP9Yc.5028G>A (p.Trp1676Ter)
n.5040G>A
c.4794G>A (p.Trp1598Ter)
c.5043G>A (p.Trp1681Ter)
Yg.12833694G>CCA414998623USP9Yc.5028G>C (p.Trp1676Cys)
n.5040G>C
c.4794G>C (p.Trp1598Cys)
c.5043G>C (p.Trp1681Cys)
Yg.12833694G>TCA414998625USP9Yc.5028G>T (p.Trp1676Cys)
n.5040G>T
c.4794G>T (p.Trp1598Cys)
c.5043G>T (p.Trp1681Cys)
Yg.12833695G>ACA414998627USP9Yc.5029G>A (p.Gly1677Ser)
n.5041G>A
c.4795G>A (p.Gly1599Ser)
c.5044G>A (p.Gly1682Ser)
Yg.12833695G>CCA414998628USP9Yc.5029G>C (p.Gly1677Arg)
n.5041G>C
c.4795G>C (p.Gly1599Arg)
c.5044G>C (p.Gly1682Arg)
Yg.12833695G>TCA414998630USP9Yc.5029G>T (p.Gly1677Cys)
n.5041G>T
c.4795G>T (p.Gly1599Cys)
c.5044G>T (p.Gly1682Cys)
Yg.12833696G>ACA414998634USP9Yc.5030G>A (p.Gly1677Asp)
n.5042G>A
c.4796G>A (p.Gly1599Asp)
c.5045G>A (p.Gly1682Asp)
Yg.12833696G>CCA414998636USP9Yc.5030G>C (p.Gly1677Ala)
n.5042G>C
c.4796G>C (p.Gly1599Ala)
c.5045G>C (p.Gly1682Ala)
Yg.12833696G>TCA414998632USP9Yc.5030G>T (p.Gly1677Val)
n.5042G>T
c.4796G>T (p.Gly1599Val)
c.5045G>T (p.Gly1682Val)
Yg.12833697T>ACA519901450USP9Yc.5031T>A (p.Gly1677=)
n.5043T>A
c.4797T>A (p.Gly1599=)
c.5046T>A (p.Gly1682=)
Yg.12833697T>CCA519901452USP9Yc.5031T>C (p.Gly1677=)
n.5043T>C
c.4797T>C (p.Gly1599=)
c.5046T>C (p.Gly1682=)
Yg.12833697T>GCA519901453USP9Yc.5031T>G (p.Gly1677=)
n.5043T>G
c.4797T>G (p.Gly1599=)
c.5046T>G (p.Gly1682=)
Yg.12833698G>ACA414998638USP9Yc.5032G>A (p.Glu1678Lys)
n.5044G>A
c.4798G>A (p.Glu1600Lys)
c.5047G>A (p.Glu1683Lys)
Yg.12833698G>CCA414998640USP9Yc.5032G>C (p.Glu1678Gln)
n.5044G>C
c.4798G>C (p.Glu1600Gln)
c.5047G>C (p.Glu1683Gln)
Yg.12833698G>TCA414998642USP9Yc.5032G>T (p.Glu1678Ter)
n.5044G>T
c.4798G>T (p.Glu1600Ter)
c.5047G>T (p.Glu1683Ter)
Yg.12833699A>CCA414998645USP9Yc.5033A>C (p.Glu1678Ala)
n.5045A>C
c.4799A>C (p.Glu1600Ala)
c.5048A>C (p.Glu1683Ala)
Yg.12833699A>GCA414998646USP9Yc.5033A>G (p.Glu1678Gly)
n.5045A>G
c.4799A>G (p.Glu1600Gly)
c.5048A>G (p.Glu1683Gly)
Yg.12833699A>TCA414998648USP9Yc.5033A>T (p.Glu1678Val)
n.5045A>T
c.4799A>T (p.Glu1600Val)
c.5048A>T (p.Glu1683Val)
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)

Number of alleles fetched