Chr Mutation (hg38) CAid Gene Transcript Linkouts
13g.108208937_108208953delCA2739277736LIG4c.2115_2131del (p.Gln706LeufsTer4)
c.2316_2332del (p.Gln773LeufsTer4)
c.2352_2368del (p.Gln785LeufsTer4)
c.2328_2344del (p.Gln777LeufsTer4)
ClinVar
13g.108208948A=CA2117793985LIG4c.2120T= (p.Leu707=)
c.2321T= (p.Leu774=)
c.2357T= (p.Leu786=)
c.2333T= (p.Leu778=)
13g.108208948A>CCA388613525LIG4c.2120T>G (p.Leu707Arg)
c.2321T>G (p.Leu774Arg)
c.2357T>G (p.Leu786Arg)
c.2333T>G (p.Leu778Arg)
13g.108208948A>GCA16609403LIG4c.2120T>C (p.Leu707Pro)
c.2321T>C (p.Leu774Pro)
c.2357T>C (p.Leu786Pro)
c.2333T>C (p.Leu778Pro)
ClinVar dbSNP gnomAD v4
13g.108208948A>TCA388613526LIG4c.2120T>A (p.Leu707Gln)
c.2321T>A (p.Leu774Gln)
c.2357T>A (p.Leu786Gln)
c.2333T>A (p.Leu778Gln)
13g.108208949G>ACA256179578LIG4c.2119C>T (p.Leu707=)
c.2320C>T (p.Leu774=)
c.2356C>T (p.Leu786=)
c.2332C>T (p.Leu778=)
ClinVar dbSNP
13g.108208949G>CCA7043524LIG4c.2119C>G (p.Leu707Val)
c.2320C>G (p.Leu774Val)
c.2356C>G (p.Leu786Val)
c.2332C>G (p.Leu778Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.108208949G=CA2117793986LIG4c.2119C= (p.Leu707=)
c.2320C= (p.Leu774=)
c.2356C= (p.Leu786=)
c.2332C= (p.Leu778=)
13g.108208949G>TCA388613527LIG4c.2119C>A (p.Leu707Met)
c.2320C>A (p.Leu774Met)
c.2356C>A (p.Leu786Met)
c.2332C>A (p.Leu778Met)
13g.108208950T>ACA388613528LIG4c.2118A>T (p.Gln706His)
c.2319A>T (p.Gln773His)
c.2355A>T (p.Gln785His)
c.2331A>T (p.Gln777His)
13g.108208950T>CCA484975421LIG4c.2118A>G (p.Gln706=)
c.2319A>G (p.Gln773=)
c.2355A>G (p.Gln785=)
c.2331A>G (p.Gln777=)
ClinVar dbSNP gnomAD v4
13g.108208950T>GCA388613529LIG4c.2118A>C (p.Gln706His)
c.2319A>C (p.Gln773His)
c.2355A>C (p.Gln785His)
c.2331A>C (p.Gln777His)
13g.108208950T=CA2117793987LIG4c.2118A= (p.Gln706=)
c.2319A= (p.Gln773=)
c.2355A= (p.Gln785=)
c.2331A= (p.Gln777=)
13g.108208951T>ACA388613530LIG4c.2117A>T (p.Gln706Leu)
c.2318A>T (p.Gln773Leu)
c.2354A>T (p.Gln785Leu)
c.2330A>T (p.Gln777Leu)
13g.108208951T>CCA388613531LIG4c.2117A>G (p.Gln706Arg)
c.2318A>G (p.Gln773Arg)
c.2354A>G (p.Gln785Arg)
c.2330A>G (p.Gln777Arg)
13g.108208951T>GCA388613532LIG4c.2117A>C (p.Gln706Pro)
c.2318A>C (p.Gln773Pro)
c.2354A>C (p.Gln785Pro)
c.2330A>C (p.Gln777Pro)
13g.108208952G>ACA388613533LIG4c.2116C>T (p.Gln706Ter)
c.2317C>T (p.Gln773Ter)
c.2353C>T (p.Gln785Ter)
c.2329C>T (p.Gln777Ter)
ClinVar dbSNP gnomAD v3 gnomAD v4
13g.108208952G>CCA388613534LIG4c.2116C>G (p.Gln706Glu)
c.2317C>G (p.Gln773Glu)
c.2353C>G (p.Gln785Glu)
c.2329C>G (p.Gln777Glu)
13g.108208952G=CA2117793988LIG4c.2116C= (p.Gln706=)
c.2317C= (p.Gln773=)
c.2353C= (p.Gln785=)
c.2329C= (p.Gln777=)
13g.108208952G>TCA388613535LIG4c.2116C>A (p.Gln706Lys)
c.2317C>A (p.Gln773Lys)
c.2353C>A (p.Gln785Lys)
c.2329C>A (p.Gln777Lys)
ClinVar dbSNP gnomAD v3 gnomAD v4
13g.108208953G>ACA256179613LIG4c.2115C>T (p.Asn705=)
c.2316C>T (p.Asn772=)
c.2352C>T (p.Asn784=)
c.2328C>T (p.Asn776=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.108208953G>CCA256179621LIG4c.2115C>G (p.Asn705Lys)
c.2316C>G (p.Asn772Lys)
c.2352C>G (p.Asn784Lys)
c.2328C>G (p.Asn776Lys)
dbSNP gnomAD v3 gnomAD v4
13g.108208953G=CA2117793989LIG4c.2115C= (p.Asn705=)
c.2316C= (p.Asn772=)
c.2352C= (p.Asn784=)
c.2328C= (p.Asn776=)
13g.108208953G>TCA388613536LIG4c.2115C>A (p.Asn705Lys)
c.2316C>A (p.Asn772Lys)
c.2352C>A (p.Asn784Lys)
c.2328C>A (p.Asn776Lys)
gnomAD v4
13g.108208954T>ACA388613537LIG4c.2114A>T (p.Asn705Ile)
c.2315A>T (p.Asn772Ile)
c.2351A>T (p.Asn784Ile)
c.2327A>T (p.Asn776Ile)
13g.108208954T>CCA388613538LIG4c.2114A>G (p.Asn705Ser)
c.2315A>G (p.Asn772Ser)
c.2351A>G (p.Asn784Ser)
c.2327A>G (p.Asn776Ser)
13g.108208954T>GCA388613539LIG4c.2114A>C (p.Asn705Thr)
c.2315A>C (p.Asn772Thr)
c.2351A>C (p.Asn784Thr)
c.2327A>C (p.Asn776Thr)
13g.108208955T>ACA7043525LIG4c.2113A>T (p.Asn705Tyr)
c.2314A>T (p.Asn772Tyr)
c.2350A>T (p.Asn784Tyr)
c.2326A>T (p.Asn776Tyr)
dbSNP ExAC gnomAD v2 gnomAD v4
13g.108208955T>CCA388613540LIG4c.2113A>G (p.Asn705Asp)
c.2314A>G (p.Asn772Asp)
c.2350A>G (p.Asn784Asp)
c.2326A>G (p.Asn776Asp)
13g.108208955T>GCA388613541LIG4c.2113A>C (p.Asn705His)
c.2314A>C (p.Asn772His)
c.2350A>C (p.Asn784His)
c.2326A>C (p.Asn776His)
13g.108208955T=CA2117793990LIG4c.2113A= (p.Asn705=)
c.2314A= (p.Asn772=)
c.2350A= (p.Asn784=)
c.2326A= (p.Asn776=)
13g.108208956C>ACA388613542LIG4c.2112G>T (p.Leu704Phe)
c.2313G>T (p.Leu771Phe)
c.2349G>T (p.Leu783Phe)
c.2325G>T (p.Leu775Phe)
13g.108208956C>GCA388613543LIG4c.2112G>C (p.Leu704Phe)
c.2313G>C (p.Leu771Phe)
c.2349G>C (p.Leu783Phe)
c.2325G>C (p.Leu775Phe)
gnomAD v4
13g.108208956C>TCA484975429LIG4c.2112G>A (p.Leu704=)
c.2313G>A (p.Leu771=)
c.2349G>A (p.Leu783=)
c.2325G>A (p.Leu775=)
13g.108208957A>CCA388613544LIG4c.2111T>G (p.Leu704Trp)
c.2312T>G (p.Leu771Trp)
c.2348T>G (p.Leu783Trp)
c.2324T>G (p.Leu775Trp)
13g.108208957A>GCA388613545LIG4c.2111T>C (p.Leu704Ser)
c.2312T>C (p.Leu771Ser)
c.2348T>C (p.Leu783Ser)
c.2324T>C (p.Leu775Ser)
13g.108208957A>TCA388613546LIG4c.2111T>A (p.Leu704Ter)
c.2312T>A (p.Leu771Ter)
c.2348T>A (p.Leu783Ter)
c.2324T>A (p.Leu775Ter)
13g.108208958A>CCA388613547LIG4c.2110T>G (p.Leu704Val)
c.2311T>G (p.Leu771Val)
c.2347T>G (p.Leu783Val)
c.2323T>G (p.Leu775Val)
13g.108208958A>GCA484975436LIG4c.2110T>C (p.Leu704=)
c.2311T>C (p.Leu771=)
c.2347T>C (p.Leu783=)
c.2323T>C (p.Leu775=)
13g.108208958A>TCA388613548LIG4c.2110T>A (p.Leu704Met)
c.2311T>A (p.Leu771Met)
c.2347T>A (p.Leu783Met)
c.2323T>A (p.Leu775Met)
13g.108208959G>ACA7043526LIG4c.2109C>T (p.Asp703=)
c.2310C>T (p.Asp770=)
c.2346C>T (p.Asp782=)
c.2322C>T (p.Asp774=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.108208959G>CCA388613549LIG4c.2109C>G (p.Asp703Glu)
c.2310C>G (p.Asp770Glu)
c.2346C>G (p.Asp782Glu)
c.2322C>G (p.Asp774Glu)
13g.108208959G=CA2117793991LIG4c.2109C= (p.Asp703=)
c.2310C= (p.Asp770=)
c.2346C= (p.Asp782=)
c.2322C= (p.Asp774=)
13g.108208959G>TCA388613550LIG4c.2109C>A (p.Asp703Glu)
c.2310C>A (p.Asp770Glu)
c.2346C>A (p.Asp782Glu)
c.2322C>A (p.Asp774Glu)
13g.108208960T>ACA388613551LIG4c.2108A>T (p.Asp703Val)
c.2309A>T (p.Asp770Val)
c.2345A>T (p.Asp782Val)
c.2321A>T (p.Asp774Val)
13g.108208960T>CCA388613552LIG4c.2108A>G (p.Asp703Gly)
c.2309A>G (p.Asp770Gly)
c.2345A>G (p.Asp782Gly)
c.2321A>G (p.Asp774Gly)
13g.108208960T>GCA388613553LIG4c.2108A>C (p.Asp703Ala)
c.2309A>C (p.Asp770Ala)
c.2345A>C (p.Asp782Ala)
c.2321A>C (p.Asp774Ala)
13g.108208961C>ACA388613554LIG4c.2107G>T (p.Asp703Tyr)
c.2308G>T (p.Asp770Tyr)
c.2344G>T (p.Asp782Tyr)
c.2320G>T (p.Asp774Tyr)
13g.108208961C>GCA388613555LIG4c.2107G>C (p.Asp703His)
c.2308G>C (p.Asp770His)
c.2344G>C (p.Asp782His)
c.2320G>C (p.Asp774His)
13g.108208961C>TCA388613556LIG4c.2107G>A (p.Asp703Asn)
c.2308G>A (p.Asp770Asn)
c.2344G>A (p.Asp782Asn)
c.2320G>A (p.Asp774Asn)

Number of alleles fetched