Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.71834363G>ACA5547878PSAPc.174+9C>T (n.174+9C>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.71834363G=CA1918891022PSAPc.174+9C= (n.174+9C=)
10g.71834364G>ACA2609589006PSAPc.174+8C>T (n.174+8C>T)
gnomAD v4
10g.71834367C=CA1918891024PSAPc.174+5G= (n.174+5G=)
10g.71834367C>TCA5547879PSAPc.174+5G>A (n.174+5G>A)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.71834370A=CA1918891025PSAPc.174+2T= (n.174+2T=)
10g.71834370A>CCA377155679PSAPc.174+2T>G (n.174+2T>G)
10g.71834370A>GCA377155681PSAPc.174+2T>C (n.174+2T>C)
dbSNP
10g.71834370A>TCA377155683PSAPc.174+2T>A (n.174+2T>A)
10g.71834371C>ACA377155684PSAPc.174+1G>T (n.174+1G>T)
10g.71834371C=CA1918891026PSAPc.174+1G= (n.174+1G=)
10g.71834371C>GCA209471778PSAPc.174+1G>C (n.174+1G>C)
dbSNP
10g.71834371C>TCA209471783PSAPc.174+1G>A (n.174+1G>A)
dbSNP
10g.71834372C>ACA470061812PSAPc.174G>T (p.Val58=)
10g.71834372C>GCA470061811PSAPc.174G>C (p.Val58=)
10g.71834372C>TCA470061809PSAPc.174G>A (p.Val58=)
10g.71834373A>CCA377155685PSAPc.173T>G (p.Val58Gly)
10g.71834373A>GCA377155687PSAPc.173T>C (p.Val58Ala)
10g.71834373A>TCA377155689PSAPc.173T>A (p.Val58Glu)
10g.71834374C>ACA377155692PSAPc.172G>T (p.Val58Leu)
10g.71834374C>GCA377155690PSAPc.172G>C (p.Val58Leu)
10g.71834374C>TCA377155691PSAPc.172G>A (p.Val58Met)
10g.71834375T>ACA470061813PSAPc.171A>T (p.Thr57=)
10g.71834375T>CCA470061814PSAPc.171A>G (p.Thr57=)
gnomAD v4
10g.71834375T>GCA470061815PSAPc.171A>C (p.Thr57=)
10g.71834376G>ACA377155693PSAPc.170C>T (p.Thr57Ile)
dbSNP gnomAD v2 gnomAD v4
10g.71834376G>CCA377155694PSAPc.170C>G (p.Thr57Arg)
dbSNP gnomAD v3 gnomAD v4
10g.71834376G=CA1918891028PSAPc.170C= (p.Thr57=)
10g.71834376G>TCA377155696PSAPc.170C>A (p.Thr57Lys)
10g.71834377T>ACA5547880PSAPc.169A>T (p.Thr57Ser)
dbSNP ExAC gnomAD v2 gnomAD v4
10g.71834377T>CCA377155701PSAPc.169A>G (p.Thr57Ala)
dbSNP gnomAD v4
10g.71834377T>GCA377155704PSAPc.169A>C (p.Thr57Pro)
10g.71834377T=CA1918891033PSAPc.169A= (p.Thr57=)
10g.71834378T>ACA470061816PSAPc.168A>T (p.Pro56=)
10g.71834378T>CCA470061817PSAPc.168A>G (p.Pro56=)
gnomAD v4
10g.71834378T>GCA470061818PSAPc.168A>C (p.Pro56=)
ClinVar dbSNP gnomAD v4
10g.71834378T=CA1918891036PSAPc.168A= (p.Pro56=)
10g.71834379G>ACA377155705PSAPc.167C>T (p.Pro56Leu)
10g.71834379G>CCA5547881PSAPc.167C>G (p.Pro56Arg)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.71834379G=CA1918891041PSAPc.167C= (p.Pro56=)
10g.71834379G>TCA377155708PSAPc.167C>A (p.Pro56Gln)
10g.71834380G>ACA209471806PSAPc.166C>T (p.Pro56Ser)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.71834380G>CCA377155711PSAPc.166C>G (p.Pro56Ala)
10g.71834380G=CA1918891043PSAPc.166C= (p.Pro56=)
10g.71834380G>TCA377155713PSAPc.166C>A (p.Pro56Thr)
10g.71834381C>ACA377155714PSAPc.165G>T (p.Lys55Asn)
dbSNP gnomAD v4
10g.71834381C=CA1918891048PSAPc.165G= (p.Lys55=)
10g.71834381C>GCA377155717PSAPc.165G>C (p.Lys55Asn)
10g.71834381C>TCA470061819PSAPc.165G>A (p.Lys55=)
gnomAD v4
10g.71834382T>ACA377155720PSAPc.164A>T (p.Lys55Met)

Number of alleles fetched