Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.39446815C>ACA356657313KLBc.2089C>A (p.Leu697Ile)
c.2062C>A (p.Leu688Ile)
4g.39446815C>GCA356657314KLBc.2089C>G (p.Leu697Val)
c.2062C>G (p.Leu688Val)
gnomAD v4
4g.39446815C>TCA439138153KLBc.2089C>T (p.Leu697=)
c.2062C>T (p.Leu688=)
4g.39446816T>ACA356657315KLBc.2090T>A (p.Leu697Gln)
c.2063T>A (p.Leu688Gln)
4g.39446816T>CCA356657316KLBc.2090T>C (p.Leu697Pro)
c.2063T>C (p.Leu688Pro)
4g.39446816T>GCA356657317KLBc.2090T>G (p.Leu697Arg)
c.2063T>G (p.Leu688Arg)
4g.39446817A>CCA439138154KLBc.2091A>C (p.Leu697=)
c.2064A>C (p.Leu688=)
4g.39446817A>GCA439138155KLBc.2091A>G (p.Leu697=)
c.2064A>G (p.Leu688=)
4g.39446817A>TCA439138156KLBc.2091A>T (p.Leu697=)
c.2064A>T (p.Leu688=)
4g.39446818A>CCA356657320KLBc.2092A>C (p.Ser698Arg)
c.2065A>C (p.Ser689Arg)
4g.39446818A>GCA356657319KLBc.2092A>G (p.Ser698Gly)
c.2065A>G (p.Ser689Gly)
4g.39446818A>TCA356657318KLBc.2092A>T (p.Ser698Cys)
c.2065A>T (p.Ser689Cys)
4g.39446819G>ACA356657321KLBc.2093G>A (p.Ser698Asn)
c.2066G>A (p.Ser689Asn)
gnomAD v4
4g.39446819G>CCA2893937KLBc.2093G>C (p.Ser698Thr)
c.2066G>C (p.Ser689Thr)
dbSNP ExAC gnomAD v3 gnomAD v4
4g.39446819G=CA1452131052KLBc.2093G= (p.Ser698=)
c.2066G= (p.Ser689=)
4g.39446819G>TCA356657322KLBc.2093G>T (p.Ser698Ile)
c.2066G>T (p.Ser689Ile)
4g.39446820T>ACA356657323KLBc.2094T>A (p.Ser698Arg)
c.2067T>A (p.Ser689Arg)
dbSNP gnomAD v2 gnomAD v4
4g.39446820T>CCA439138158KLBc.2094T>C (p.Ser698=)
c.2067T>C (p.Ser689=)
4g.39446820T>GCA356657324KLBc.2094T>G (p.Ser698Arg)
c.2067T>G (p.Ser689Arg)
4g.39446820T=CA1452131053KLBc.2094T= (p.Ser698=)
c.2067T= (p.Ser689=)
4g.39446821G>ACA356657325KLBc.2095G>A (p.Asp699Asn)
c.2068G>A (p.Asp690Asn)
dbSNP
4g.39446821G>CCA356657326KLBc.2095G>C (p.Asp699His)
c.2068G>C (p.Asp690His)
4g.39446821G=CA1452131054KLBc.2095G= (p.Asp699=)
c.2068G= (p.Asp690=)
4g.39446821G>TCA356657327KLBc.2095G>T (p.Asp699Tyr)
c.2068G>T (p.Asp690Tyr)
gnomAD v4
4g.39446822A>CCA356657328KLBc.2096A>C (p.Asp699Ala)
c.2069A>C (p.Asp690Ala)
4g.39446822A>GCA356657329KLBc.2096A>G (p.Asp699Gly)
c.2069A>G (p.Asp690Gly)
4g.39446822A>TCA356657330KLBc.2096A>T (p.Asp699Val)
c.2069A>T (p.Asp690Val)
4g.39446823C>ACA356657331KLBc.2097C>A (p.Asp699Glu)
c.2070C>A (p.Asp690Glu)
4g.39446823C>GCA356657332KLBc.2097C>G (p.Asp699Glu)
c.2070C>G (p.Asp690Glu)
4g.39446823C>TCA439138161KLBc.2097C>T (p.Asp699=)
c.2070C>T (p.Asp690=)
4g.39446824A>CCA356657335KLBc.2098A>C (p.Ile700Leu)
c.2071A>C (p.Ile691Leu)
4g.39446824A>GCA356657334KLBc.2098A>G (p.Ile700Val)
c.2071A>G (p.Ile691Val)
4g.39446824A>TCA356657333KLBc.2098A>T (p.Ile700Phe)
c.2071A>T (p.Ile691Phe)
4g.39446825T>ACA356657336KLBc.2099T>A (p.Ile700Asn)
c.2072T>A (p.Ile691Asn)
4g.39446825T>CCA356657337KLBc.2099T>C (p.Ile700Thr)
c.2072T>C (p.Ile691Thr)
4g.39446825T>GCA356657338KLBc.2099T>G (p.Ile700Ser)
c.2072T>G (p.Ile691Ser)
4g.39446826C>ACA95711785KLBc.2100C>A (p.Ile700=)
c.2073C>A (p.Ile691=)
dbSNP gnomAD v3 gnomAD v4
4g.39446826C=CA1452131055KLBc.2100C= (p.Ile700=)
c.2073C= (p.Ile691=)
4g.39446826C>GCA356657339KLBc.2100C>G (p.Ile700Met)
c.2073C>G (p.Ile691Met)
gnomAD v4
4g.39446826C>TCA2893938KLBc.2100C>T (p.Ile700=)
c.2073C>T (p.Ile691=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.39446827T>ACA356657340KLBc.2101T>A (p.Tyr701Asn)
c.2074T>A (p.Tyr692Asn)
4g.39446827T>CCA356657341KLBc.2101T>C (p.Tyr701His)
c.2074T>C (p.Tyr692His)
4g.39446827T>GCA356657342KLBc.2101T>G (p.Tyr701Asp)
c.2074T>G (p.Tyr692Asp)
4g.39446828A>CCA356657343KLBc.2102A>C (p.Tyr701Ser)
c.2075A>C (p.Tyr692Ser)
4g.39446828A>GCA356657344KLBc.2102A>G (p.Tyr701Cys)
c.2075A>G (p.Tyr692Cys)
4g.39446828A>TCA356657345KLBc.2102A>T (p.Tyr701Phe)
c.2075A>T (p.Tyr692Phe)
4g.39446829C>ACA356657346KLBc.2103C>A (p.Tyr701Ter)
c.2076C>A (p.Tyr692Ter)
4g.39446829C=CA1452131056KLBc.2103C= (p.Tyr701=)
c.2076C= (p.Tyr692=)
4g.39446829C>GCA356657347KLBc.2103C>G (p.Tyr701Ter)
c.2076C>G (p.Tyr692Ter)
4g.39446829C>TCA2893939KLBc.2103C>T (p.Tyr701=)
c.2076C>T (p.Tyr692=)
dbSNP ExAC gnomAD v2 gnomAD v4

Number of alleles fetched