Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.38774559C>ACA2888990TLR10c.1032G>T (p.Pro344=)
c.990G>T (p.Pro330=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.38774559C=CA1451835898TLR10c.1032G= (p.Pro344=)
c.990G= (p.Pro330=)
4g.38774559C>GCA439132340TLR10c.1032G>C (p.Pro344=)
c.990G>C (p.Pro330=)
4g.38774559C>TCA2888991TLR10c.1032G>A (p.Pro344=)
c.990G>A (p.Pro330=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
4g.38774560G>ACA2888992TLR10c.1031C>T (p.Pro344Leu)
c.989C>T (p.Pro330Leu)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.38774560G>CCA356605051TLR10c.1031C>G (p.Pro344Arg)
c.989C>G (p.Pro330Arg)
4g.38774560G=CA1451835903TLR10c.1031C= (p.Pro344=)
c.989C= (p.Pro330=)
4g.38774560G>TCA356605052TLR10c.1031C>A (p.Pro344Gln)
c.989C>A (p.Pro330Gln)
4g.38774561G>ACA356605053TLR10c.1030C>T (p.Pro344Ser)
c.988C>T (p.Pro330Ser)
COSMIC
4g.38774561G>CCA356605054TLR10c.1030C>G (p.Pro344Ala)
c.988C>G (p.Pro330Ala)
dbSNP
4g.38774561G=CA1451835907TLR10c.1030C= (p.Pro344=)
c.988C= (p.Pro330=)
4g.38774561G>TCA356605055TLR10c.1030C>A (p.Pro344Thr)
c.988C>A (p.Pro330Thr)
4g.38774562G>ACA439132341TLR10c.1029C>T (p.Phe343=)
c.987C>T (p.Phe329=)
4g.38774562G>CCA356605056TLR10c.1029C>G (p.Phe343Leu)
c.987C>G (p.Phe329Leu)
4g.38774562G>TCA356605057TLR10c.1029C>A (p.Phe343Leu)
c.987C>A (p.Phe329Leu)
gnomAD v4
4g.38774563A>CCA356605058TLR10c.1028T>G (p.Phe343Cys)
c.986T>G (p.Phe329Cys)
4g.38774563A>GCA356605060TLR10c.1028T>C (p.Phe343Ser)
c.986T>C (p.Phe329Ser)
4g.38774563A>TCA356605059TLR10c.1028T>A (p.Phe343Tyr)
c.986T>A (p.Phe329Tyr)
4g.38774566delCA2670339572TLR10c.1028del (p.Phe343SerfsTer11)
c.986del (p.Phe329SerfsTer11)
gnomAD v4
4g.38774564A>CCA356605061TLR10c.1027T>G (p.Phe343Val)
c.985T>G (p.Phe329Val)
4g.38774564A>GCA356605062TLR10c.1027T>C (p.Phe343Leu)
c.985T>C (p.Phe329Leu)
4g.38774564A>TCA356605063TLR10c.1027T>A (p.Phe343Ile)
c.985T>A (p.Phe329Ile)
4g.38774565A=CA1451835911TLR10c.1026T= (p.Leu342=)
c.984T= (p.Leu328=)
4g.38774565A>CCA439132342TLR10c.1026T>G (p.Leu342=)
c.984T>G (p.Leu328=)
4g.38774565A>GCA439132344TLR10c.1026T>C (p.Leu342=)
c.984T>C (p.Leu328=)
dbSNP gnomAD v2
4g.38774565A>TCA439132343TLR10c.1026T>A (p.Leu342=)
c.984T>A (p.Leu328=)
4g.38774566A>CCA356605064TLR10c.1025T>G (p.Leu342Arg)
c.983T>G (p.Leu328Arg)
4g.38774566A>GCA356605065TLR10c.1025T>C (p.Leu342Pro)
c.983T>C (p.Leu328Pro)
4g.38774566A>TCA356605066TLR10c.1025T>A (p.Leu342His)
c.983T>A (p.Leu328His)
4g.38774567G>ACA356605067TLR10c.1024C>T (p.Leu342Phe)
c.982C>T (p.Leu328Phe)
4g.38774567G>CCA356605068TLR10c.1024C>G (p.Leu342Val)
c.982C>G (p.Leu328Val)
dbSNP gnomAD v2 gnomAD v4
4g.38774567G=CA1451835926TLR10c.1024C= (p.Leu342=)
c.982C= (p.Leu328=)
4g.38774567G>TCA356605069TLR10c.1024C>A (p.Leu342Ile)
c.982C>A (p.Leu328Ile)
4g.38774568C>ACA356605070TLR10c.1023G>T (p.Met341Ile)
c.981G>T (p.Met327Ile)
4g.38774568C>GCA356605071TLR10c.1023G>C (p.Met341Ile)
c.981G>C (p.Met327Ile)
4g.38774568C>TCA356605072TLR10c.1023G>A (p.Met341Ile)
c.981G>A (p.Met327Ile)
gnomAD v4
4g.38774569A=CA1451835944TLR10c.1022T= (p.Met341=)
c.980T= (p.Met327=)
4g.38774569A>CCA356605075TLR10c.1022T>G (p.Met341Arg)
c.980T>G (p.Met327Arg)
gnomAD v4
4g.38774569A>GCA356605073TLR10c.1022T>C (p.Met341Thr)
c.980T>C (p.Met327Thr)
dbSNP gnomAD v4
4g.38774569A>TCA356605074TLR10c.1022T>A (p.Met341Lys)
c.980T>A (p.Met327Lys)
dbSNP
4g.38774570T>ACA356605076TLR10c.1021A>T (p.Met341Leu)
c.979A>T (p.Met327Leu)
4g.38774570T>CCA356605077TLR10c.1021A>G (p.Met341Val)
c.979A>G (p.Met327Val)
gnomAD v4
4g.38774570T>GCA356605078TLR10c.1021A>C (p.Met341Leu)
c.979A>C (p.Met327Leu)
4g.38774571G>ACA95623024TLR10c.1020C>T (p.His340=)
c.978C>T (p.His326=)
dbSNP gnomAD v2 gnomAD v4
4g.38774571G>CCA356605079TLR10c.1020C>G (p.His340Gln)
c.978C>G (p.His326Gln)
4g.38774571G=CA1451835949TLR10c.1020C= (p.His340=)
c.978C= (p.His326=)
4g.38774571G>TCA356605080TLR10c.1020C>A (p.His340Gln)
c.978C>A (p.His326Gln)
4g.38774572T>ACA356605083TLR10c.1019A>T (p.His340Leu)
c.977A>T (p.His326Leu)
4g.38774572T>CCA356605082TLR10c.1019A>G (p.His340Arg)
c.977A>G (p.His326Arg)
4g.38774572T>GCA356605081TLR10c.1019A>C (p.His340Pro)
c.977A>C (p.His326Pro)
gnomAD v4

Number of alleles fetched