Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.125317649A>CCA358117490FAT4c.1238A>C (p.Lys413Thr)
c.-55+1672A>C (n.-55+1672A>C)
4g.125317649A>GCA358117491FAT4c.1238A>G (p.Lys413Arg)
c.-55+1672A>G (n.-55+1672A>G)
4g.125317649A>TCA358117492FAT4c.1238A>T (p.Lys413Ile)
c.-55+1672A>T (n.-55+1672A>T)
4g.125317650A>CCA358117493FAT4c.1239A>C (p.Lys413Asn)
c.-55+1673A>C (n.-55+1673A>C)
4g.125317650A>GCA441366875FAT4c.1239A>G (p.Lys413=)
c.-55+1673A>G (n.-55+1673A>G)
4g.125317650A>TCA358117494FAT4c.1239A>T (p.Lys413Asn)
c.-55+1673A>T (n.-55+1673A>T)
4g.125317651G>ACA358117495FAT4c.1240G>A (p.Val414Met)
c.-55+1674G>A (n.-55+1674G>A)
4g.125317651G>CCA358117496FAT4c.1240G>C (p.Val414Leu)
c.-55+1674G>C (n.-55+1674G>C)
gnomAD v4
4g.125317651G>TCA358117497FAT4c.1240G>T (p.Val414Leu)
c.-55+1674G>T (n.-55+1674G>T)
4g.125317652T>ACA358117499FAT4c.1241T>A (p.Val414Glu)
c.-55+1675T>A (n.-55+1675T>A)
4g.125317652T>CCA3071946FAT4c.1241T>C (p.Val414Ala)
c.-55+1675T>C (n.-55+1675T>C)
dbSNP ExAC gnomAD v2
4g.125317652T>GCA358117498FAT4c.1241T>G (p.Val414Gly)
c.-55+1675T>G (n.-55+1675T>G)
4g.125317652T=CA1491600364FAT4c.1241T= (p.Val414=)
c.-55+1675T= (n.-55+1675T=)
4g.125317653G>ACA441366887FAT4c.1242G>A (p.Val414=)
c.-55+1676G>A (n.-55+1676G>A)
4g.125317653G>CCA441366889FAT4c.1242G>C (p.Val414=)
c.-55+1676G>C (n.-55+1676G>C)
4g.125317653G>TCA441366890FAT4c.1242G>T (p.Val414=)
c.-55+1676G>T (n.-55+1676G>T)
4g.125317654C>ACA358117501FAT4c.1243C>A (p.Pro415Thr)
c.-55+1677C>A (n.-55+1677C>A)
4g.125317654C>GCA358117500FAT4c.1243C>G (p.Pro415Ala)
c.-55+1677C>G (n.-55+1677C>G)
4g.125317654C>TCA358117502FAT4c.1243C>T (p.Pro415Ser)
c.-55+1677C>T (n.-55+1677C>T)
gnomAD v4 COSMIC COSMIC
4g.125317655C>ACA358117503FAT4c.1244C>A (p.Pro415Gln)
c.-55+1678C>A (n.-55+1678C>A)
4g.125317655C=CA1491600368FAT4c.1244C= (p.Pro415=)
c.-55+1678C= (n.-55+1678C=)
4g.125317655C>GCA3071947FAT4c.1244C>G (p.Pro415Arg)
c.-55+1678C>G (n.-55+1678C>G)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.125317655C>TCA104862065FAT4c.1244C>T (p.Pro415Leu)
c.-55+1678C>T (n.-55+1678C>T)
dbSNP
4g.125317656G>ACA441366900FAT4c.1245G>A (p.Pro415=)
c.-55+1679G>A (n.-55+1679G>A)
dbSNP COSMIC COSMIC
4g.125317656G>CCA441366901FAT4c.1245G>C (p.Pro415=)
c.-55+1679G>C (n.-55+1679G>C)
4g.125317656G=CA1491600376FAT4c.1245G= (p.Pro415=)
c.-55+1679G= (n.-55+1679G=)
4g.125317656G>TCA441366902FAT4c.1245G>T (p.Pro415=)
c.-55+1679G>T (n.-55+1679G>T)
ClinVar dbSNP gnomAD v4
4g.125317657A>CCA358117504FAT4c.1246A>C (p.Asn416His)
c.-55+1680A>C (n.-55+1680A>C)
4g.125317657A>GCA358117506FAT4c.1246A>G (p.Asn416Asp)
c.-55+1680A>G (n.-55+1680A>G)
4g.125317657A>TCA358117505FAT4c.1246A>T (p.Asn416Tyr)
c.-55+1680A>T (n.-55+1680A>T)
4g.125317658A>CCA358117507FAT4c.1247A>C (p.Asn416Thr)
c.-55+1681A>C (n.-55+1681A>C)
4g.125317658A>GCA358117508FAT4c.1247A>G (p.Asn416Ser)
c.-55+1681A>G (n.-55+1681A>G)
4g.125317658A>TCA358117509FAT4c.1247A>T (p.Asn416Ile)
c.-55+1681A>T (n.-55+1681A>T)
4g.125317659C>ACA358117510FAT4c.1248C>A (p.Asn416Lys)
c.-55+1682C>A (n.-55+1682C>A)
4g.125317659C=CA1491600381FAT4c.1248C= (p.Asn416=)
c.-55+1682C= (n.-55+1682C=)
4g.125317659C>GCA358117511FAT4c.1248C>G (p.Asn416Lys)
c.-55+1682C>G (n.-55+1682C>G)
4g.125317659C>TCA3071948FAT4c.1248C>T (p.Asn416=)
c.-55+1682C>T (n.-55+1682C>T)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.125317660C>ACA358117512FAT4c.1249C>A (p.Leu417Met)
c.-55+1683C>A (n.-55+1683C>A)
4g.125317660C=CA1491600394FAT4c.1249C= (p.Leu417=)
c.-55+1683C= (n.-55+1683C=)
4g.125317660C>GCA358117513FAT4c.1249C>G (p.Leu417Val)
c.-55+1683C>G (n.-55+1683C>G)
4g.125317660C>TCA441366916FAT4c.1249C>T (p.Leu417=)
c.-55+1683C>T (n.-55+1683C>T)
dbSNP
4g.125317661T>ACA358117514FAT4c.1250T>A (p.Leu417Gln)
c.-55+1684T>A (n.-55+1684T>A)
4g.125317661T>CCA358117515FAT4c.1250T>C (p.Leu417Pro)
c.-55+1684T>C (n.-55+1684T>C)
dbSNP
4g.125317661T>GCA358117516FAT4c.1250T>G (p.Leu417Arg)
c.-55+1684T>G (n.-55+1684T>G)
4g.125317661T=CA1491600403FAT4c.1250T= (p.Leu417=)
c.-55+1684T= (n.-55+1684T=)
4g.125317662G>ACA441366922FAT4c.1251G>A (p.Leu417=)
c.-55+1685G>A (n.-55+1685G>A)
4g.125317662G>CCA441366920FAT4c.1251G>C (p.Leu417=)
c.-55+1685G>C (n.-55+1685G>C)
4g.125317662G>TCA441366918FAT4c.1251G>T (p.Leu417=)
c.-55+1685G>T (n.-55+1685G>T)
4g.125317663A=CA1491600407FAT4c.1252A= (p.Ser418=)
c.-55+1686A= (n.-55+1686A=)
4g.125317663A>CCA358117519FAT4c.1252A>C (p.Ser418Arg)
c.-55+1686A>C (n.-55+1686A>C)

Number of alleles fetched