Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.209615280G>ACA423027975LAMB3c.3510C>T (p.Thr1170=)
c.3318C>T (p.Thr1106=)
1g.209615280G>CCA423027976LAMB3c.3510C>G (p.Thr1170=)
c.3318C>G (p.Thr1106=)
1g.209615280G>TCA423027978LAMB3c.3510C>A (p.Thr1170=)
c.3318C>A (p.Thr1106=)
1g.209615281G>ACA344580515LAMB3c.3509C>T (p.Thr1170Ile)
c.3317C>T (p.Thr1106Ile)
1g.209615281G>CCA344580521LAMB3c.3509C>G (p.Thr1170Ser)
c.3317C>G (p.Thr1106Ser)
1g.209615281G>TCA344580523LAMB3c.3509C>A (p.Thr1170Asn)
c.3317C>A (p.Thr1106Asn)
1g.209615282T>ACA344580529LAMB3c.3508A>T (p.Thr1170Ser)
c.3316A>T (p.Thr1106Ser)
1g.209615282T>CCA344580531LAMB3c.3508A>G (p.Thr1170Ala)
c.3316A>G (p.Thr1106Ala)
1g.209615282T>GCA344580527LAMB3c.3508A>C (p.Thr1170Pro)
c.3316A>C (p.Thr1106Pro)
1g.209615283G>ACA423027994LAMB3c.3507C>T (p.Ala1169=)
c.3315C>T (p.Ala1105=)
ClinVar
1g.209615283G>CCA423027997LAMB3c.3507C>G (p.Ala1169=)
c.3315C>G (p.Ala1105=)
1g.209615283G>TCA423027999LAMB3c.3507C>A (p.Ala1169=)
c.3315C>A (p.Ala1105=)
1g.209615284G>ACA36742922LAMB3c.3506C>T (p.Ala1169Val)
c.3314C>T (p.Ala1105Val)
dbSNP gnomAD v4
1g.209615284G>CCA344580533LAMB3c.3506C>G (p.Ala1169Gly)
c.3314C>G (p.Ala1105Gly)
1g.209615284G=CA2484294989LAMB3c.3506C= (p.Ala1169=)
c.3314C= (p.Ala1105=)
1g.209615284G>TCA344580534LAMB3c.3506C>A (p.Ala1169Asp)
c.3314C>A (p.Ala1105Asp)
1g.209615285C>ACA344580536LAMB3c.3505G>T (p.Ala1169Ser)
c.3313G>T (p.Ala1105Ser)
1g.209615285C>GCA344580547LAMB3c.3505G>C (p.Ala1169Pro)
c.3313G>C (p.Ala1105Pro)
1g.209615285C>TCA344580548LAMB3c.3505G>A (p.Ala1169Thr)
c.3313G>A (p.Ala1105Thr)
1g.209615286A>CCA344580550LAMB3c.3504T>G (p.Tyr1168Ter)
c.3312T>G (p.Tyr1104Ter)
gnomAD v4
1g.209615286A>GCA423028018LAMB3c.3504T>C (p.Tyr1168=)
c.3312T>C (p.Tyr1104=)
1g.209615286A>TCA344580549LAMB3c.3504T>A (p.Tyr1168Ter)
c.3312T>A (p.Tyr1104Ter)
1g.209615287T>ACA344580551LAMB3c.3503A>T (p.Tyr1168Phe)
c.3311A>T (p.Tyr1104Phe)
1g.209615287T>CCA344580552LAMB3c.3503A>G (p.Tyr1168Cys)
c.3311A>G (p.Tyr1104Cys)
gnomAD v4
1g.209615287T>GCA344580553LAMB3c.3503A>C (p.Tyr1168Ser)
c.3311A>C (p.Tyr1104Ser)
dbSNP
1g.209615287T=CA2484294990LAMB3c.3503A= (p.Tyr1168=)
c.3311A= (p.Tyr1104=)
1g.209615288A>CCA344580554LAMB3c.3502T>G (p.Tyr1168Asp)
c.3310T>G (p.Tyr1104Asp)
1g.209615288A>GCA344580555LAMB3c.3502T>C (p.Tyr1168His)
c.3310T>C (p.Tyr1104His)
1g.209615288A>TCA344580556LAMB3c.3502T>A (p.Tyr1168Asn)
c.3310T>A (p.Tyr1104Asn)
1g.209615289G>ACA1374834LAMB3c.3501C>T (p.Tyr1167=)
c.3309C>T (p.Tyr1103=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.209615289G>CCA344580557LAMB3c.3501C>G (p.Tyr1167Ter)
c.3309C>G (p.Tyr1103Ter)
1g.209615289G=CA2484294991LAMB3c.3501C= (p.Tyr1167=)
c.3309C= (p.Tyr1103=)
1g.209615289G>TCA344580558LAMB3c.3501C>A (p.Tyr1167Ter)
c.3309C>A (p.Tyr1103Ter)
1g.209615290T>ACA344580559LAMB3c.3500A>T (p.Tyr1167Phe)
c.3308A>T (p.Tyr1103Phe)
1g.209615290T>CCA344580560LAMB3c.3500A>G (p.Tyr1167Cys)
c.3308A>G (p.Tyr1103Cys)
1g.209615290T>GCA344580561LAMB3c.3500A>C (p.Tyr1167Ser)
c.3308A>C (p.Tyr1103Ser)
1g.209615291A>CCA344580562LAMB3c.3499T>G (p.Tyr1167Asp)
c.3307T>G (p.Tyr1103Asp)
1g.209615291A>GCA344580563LAMB3c.3499T>C (p.Tyr1167His)
c.3307T>C (p.Tyr1103His)
1g.209615291A>TCA344580564LAMB3c.3499T>A (p.Tyr1167Asn)
c.3307T>A (p.Tyr1103Asn)
1g.209615292G>ACA36742931LAMB3c.3498C>T (p.Leu1166=)
c.3306C>T (p.Leu1102=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
1g.209615292G>CCA1374835LAMB3c.3498C>G (p.Leu1166=)
c.3306C>G (p.Leu1102=)
dbSNP ExAC gnomAD v2
1g.209615292G=CA2484294992LAMB3c.3498C= (p.Leu1166=)
c.3306C= (p.Leu1102=)
1g.209615292G>TCA423028049LAMB3c.3498C>A (p.Leu1166=)
c.3306C>A (p.Leu1102=)
1g.209615293A>CCA344580565LAMB3c.3497T>G (p.Leu1166Arg)
c.3305T>G (p.Leu1102Arg)
1g.209615293A>GCA344580566LAMB3c.3497T>C (p.Leu1166Pro)
c.3305T>C (p.Leu1102Pro)
1g.209615293A>TCA344580567LAMB3c.3497T>A (p.Leu1166His)
c.3305T>A (p.Leu1102His)
1g.209615294G>ACA344580568LAMB3c.3496C>T (p.Leu1166Phe)
c.3304C>T (p.Leu1102Phe)
1g.209615294G>CCA344580571LAMB3c.3496C>G (p.Leu1166Val)
c.3304C>G (p.Leu1102Val)
1g.209615294G>TCA344580573LAMB3c.3496C>A (p.Leu1166Ile)
c.3304C>A (p.Leu1102Ile)
1g.209615295C>ACA423028069LAMB3c.3495G>T (p.Val1165=)
c.3303G>T (p.Val1101=)

Number of alleles fetched