Chr Mutation (hg38) CAid Gene Transcript Linkouts
13g.108211146T>ACA388624448LIG4c.-79A>T (n.-79A>T)
c.123A>T (p.Glu41Asp)
c.159A>T (p.Glu53Asp)
c.135A>T (p.Glu45Asp)
13g.108211146T>CCA484976303LIG4c.-79A>G (n.-79A>G)
c.123A>G (p.Glu41=)
c.159A>G (p.Glu53=)
c.135A>G (p.Glu45=)
13g.108211146T>GCA388624449LIG4c.-79A>C (n.-79A>C)
c.123A>C (p.Glu41Asp)
c.159A>C (p.Glu53Asp)
c.135A>C (p.Glu45Asp)
13g.108211147T>ACA388624452LIG4c.-80A>T (n.-80A>T)
c.122A>T (p.Glu41Val)
c.158A>T (p.Glu53Val)
c.134A>T (p.Glu45Val)
13g.108211147T>CCA388624455LIG4c.-80A>G (n.-80A>G)
c.122A>G (p.Glu41Gly)
c.158A>G (p.Glu53Gly)
c.134A>G (p.Glu45Gly)
13g.108211147T>GCA388624456LIG4c.-80A>C (n.-80A>C)
c.122A>C (p.Glu41Ala)
c.158A>C (p.Glu53Ala)
c.134A>C (p.Glu45Ala)
13g.108211148C>ACA388624459LIG4c.-81G>T (n.-81G>T)
c.121G>T (p.Glu41Ter)
c.157G>T (p.Glu53Ter)
c.133G>T (p.Glu45Ter)
13g.108211148C>GCA388624464LIG4c.-81G>C (n.-81G>C)
c.121G>C (p.Glu41Gln)
c.157G>C (p.Glu53Gln)
c.133G>C (p.Glu45Gln)
13g.108211148C>TCA388624461LIG4c.-81G>A (n.-81G>A)
c.121G>A (p.Glu41Lys)
c.157G>A (p.Glu53Lys)
c.133G>A (p.Glu45Lys)
13g.108211149C>ACA388624466LIG4c.-82G>T (n.-82G>T)
c.120G>T (p.Arg40Ser)
c.156G>T (p.Arg52Ser)
c.132G>T (p.Arg44Ser)
13g.108211149C>GCA388624469LIG4c.-82G>C (n.-82G>C)
c.120G>C (p.Arg40Ser)
c.156G>C (p.Arg52Ser)
c.132G>C (p.Arg44Ser)
13g.108211149C>TCA484976307LIG4c.-82G>A (n.-82G>A)
c.120G>A (p.Arg40=)
c.156G>A (p.Arg52=)
c.132G>A (p.Arg44=)
13g.108211150C>ACA388624472LIG4c.-83G>T (n.-83G>T)
c.119G>T (p.Arg40Met)
c.155G>T (p.Arg52Met)
c.131G>T (p.Arg44Met)
13g.108211150C>GCA388624474LIG4c.-83G>C (n.-83G>C)
c.119G>C (p.Arg40Thr)
c.155G>C (p.Arg52Thr)
c.131G>C (p.Arg44Thr)
13g.108211150C>TCA388624477LIG4c.-83G>A (n.-83G>A)
c.119G>A (p.Arg40Lys)
c.155G>A (p.Arg52Lys)
c.131G>A (p.Arg44Lys)
gnomAD v3 gnomAD v4
13g.108211151T>ACA388624479LIG4c.-84A>T (n.-84A>T)
c.118A>T (p.Arg40Trp)
c.154A>T (p.Arg52Trp)
c.130A>T (p.Arg44Trp)
13g.108211151T>CCA388624480LIG4c.-84A>G (n.-84A>G)
c.118A>G (p.Arg40Gly)
c.154A>G (p.Arg52Gly)
c.130A>G (p.Arg44Gly)
dbSNP gnomAD v2 gnomAD v4
13g.108211151T>GCA484976308LIG4c.-84A>C (n.-84A>C)
c.118A>C (p.Arg40=)
c.154A>C (p.Arg52=)
c.130A>C (p.Arg44=)
13g.108211151T=CA2117794896LIG4c.-84A= (n.-84A=)
c.118A= (p.Arg40=)
c.154A= (p.Arg52=)
c.130A= (p.Arg44=)
13g.108211152G>ACA484976309LIG4c.-85C>T (n.-85C>T)
c.117C>T (p.Phe39=)
c.153C>T (p.Phe51=)
c.129C>T (p.Phe43=)
COSMIC
13g.108211152G>CCA388624482LIG4c.-85C>G (n.-85C>G)
c.117C>G (p.Phe39Leu)
c.153C>G (p.Phe51Leu)
c.129C>G (p.Phe43Leu)
dbSNP gnomAD v2 gnomAD v4
13g.108211152G=CA2117794897LIG4c.-85C= (n.-85C=)
c.117C= (p.Phe39=)
c.153C= (p.Phe51=)
c.129C= (p.Phe43=)
13g.108211152G>TCA388624483LIG4c.-85C>A (n.-85C>A)
c.117C>A (p.Phe39Leu)
c.153C>A (p.Phe51Leu)
c.129C>A (p.Phe43Leu)
ClinVar dbSNP
13g.108211153A>CCA388624486LIG4c.-86T>G (n.-86T>G)
c.116T>G (p.Phe39Cys)
c.152T>G (p.Phe51Cys)
c.128T>G (p.Phe43Cys)
ClinVar
13g.108211153A>GCA388624489LIG4c.-86T>C (n.-86T>C)
c.116T>C (p.Phe39Ser)
c.152T>C (p.Phe51Ser)
c.128T>C (p.Phe43Ser)
13g.108211153A>TCA388624492LIG4c.-86T>A (n.-86T>A)
c.116T>A (p.Phe39Tyr)
c.152T>A (p.Phe51Tyr)
c.128T>A (p.Phe43Tyr)
13g.108211154A>CCA388624497LIG4c.-87T>G (n.-87T>G)
c.115T>G (p.Phe39Val)
c.151T>G (p.Phe51Val)
c.127T>G (p.Phe43Val)
gnomAD v4
13g.108211154A>GCA388624494LIG4c.-87T>C (n.-87T>C)
c.115T>C (p.Phe39Leu)
c.151T>C (p.Phe51Leu)
c.127T>C (p.Phe43Leu)
13g.108211154A>TCA388624496LIG4c.-87T>A (n.-87T>A)
c.115T>A (p.Phe39Ile)
c.151T>A (p.Phe51Ile)
c.127T>A (p.Phe43Ile)
13g.108211155G>ACA484976311LIG4c.-88C>T (n.-88C>T)
c.114C>T (p.His38=)
c.150C>T (p.His50=)
c.126C>T (p.His42=)
13g.108211155G>CCA388624498LIG4c.-88C>G (n.-88C>G)
c.114C>G (p.His38Gln)
c.150C>G (p.His50Gln)
c.126C>G (p.His42Gln)
13g.108211155G>TCA388624499LIG4c.-88C>A (n.-88C>A)
c.114C>A (p.His38Gln)
c.150C>A (p.His50Gln)
c.126C>A (p.His42Gln)
13g.108211156T>ACA388624501LIG4c.-89A>T (n.-89A>T)
c.113A>T (p.His38Leu)
c.149A>T (p.His50Leu)
c.125A>T (p.His42Leu)
13g.108211156T>CCA388624503LIG4c.-89A>G (n.-89A>G)
c.113A>G (p.His38Arg)
c.149A>G (p.His50Arg)
c.125A>G (p.His42Arg)
13g.108211156T>GCA388624505LIG4c.-89A>C (n.-89A>C)
c.113A>C (p.His38Pro)
c.149A>C (p.His50Pro)
c.125A>C (p.His42Pro)
13g.108211157G>ACA388624508LIG4c.-90C>T (n.-90C>T)
c.112C>T (p.His38Tyr)
c.148C>T (p.His50Tyr)
c.124C>T (p.His42Tyr)
gnomAD v4
13g.108211157G>CCA388624513LIG4c.-90C>G (n.-90C>G)
c.112C>G (p.His38Asp)
c.148C>G (p.His50Asp)
c.124C>G (p.His42Asp)
13g.108211157G>TCA388624515LIG4c.-90C>A (n.-90C>A)
c.112C>A (p.His38Asn)
c.148C>A (p.His50Asn)
c.124C>A (p.His42Asn)
13g.108211158T>ACA388624517LIG4c.-91A>T (n.-91A>T)
c.111A>T (p.Arg37Ser)
c.147A>T (p.Arg49Ser)
c.123A>T (p.Arg41Ser)
13g.108211158T>CCA484976314LIG4c.-91A>G (n.-91A>G)
c.111A>G (p.Arg37=)
c.147A>G (p.Arg49=)
c.123A>G (p.Arg41=)
13g.108211158T>GCA388624518LIG4c.-91A>C (n.-91A>C)
c.111A>C (p.Arg37Ser)
c.147A>C (p.Arg49Ser)
c.123A>C (p.Arg41Ser)
13g.108211159C>ACA388624521LIG4c.-92G>T (n.-92G>T)
c.110G>T (p.Arg37Ile)
c.146G>T (p.Arg49Ile)
c.122G>T (p.Arg41Ile)
13g.108211159C>GCA388624524LIG4c.-92G>C (n.-92G>C)
c.110G>C (p.Arg37Thr)
c.146G>C (p.Arg49Thr)
c.122G>C (p.Arg41Thr)
13g.108211159C>TCA388624527LIG4c.-92G>A (n.-92G>A)
c.110G>A (p.Arg37Lys)
c.146G>A (p.Arg49Lys)
c.122G>A (p.Arg41Lys)
13g.108211160T>ACA388624532LIG4c.-93A>T (n.-93A>T)
c.109A>T (p.Arg37Ter)
c.145A>T (p.Arg49Ter)
c.121A>T (p.Arg41Ter)
gnomAD v4 COSMIC
13g.108211160T>CCA388624529LIG4c.-93A>G (n.-93A>G)
c.109A>G (p.Arg37Gly)
c.145A>G (p.Arg49Gly)
c.121A>G (p.Arg41Gly)
13g.108211160T>GCA484976316LIG4c.-93A>C (n.-93A>C)
c.109A>C (p.Arg37=)
c.145A>C (p.Arg49=)
c.121A>C (p.Arg41=)
13g.108211161G>ACA484976317LIG4c.-94C>T (n.-94C>T)
c.108C>T (p.Ile36=)
c.144C>T (p.Ile48=)
c.120C>T (p.Ile40=)
13g.108211161G>CCA388624534LIG4c.-94C>G (n.-94C>G)
c.108C>G (p.Ile36Met)
c.144C>G (p.Ile48Met)
c.120C>G (p.Ile40Met)
ClinVar dbSNP gnomAD v3 gnomAD v4
13g.108211161G=CA2117794898LIG4c.-94C= (n.-94C=)
c.108C= (p.Ile36=)
c.144C= (p.Ile48=)
c.120C= (p.Ile40=)

Number of alleles fetched