Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.209618569T>ACA344585187LAMB3c.2792A>T (p.Lys931Met)
c.-2A>T (n.-2A>T)
c.2600A>T (p.Lys867Met)
1g.209618569T>CCA344585188LAMB3c.2792A>G (p.Lys931Arg)
c.-2A>G (n.-2A>G)
c.2600A>G (p.Lys867Arg)
1g.209618569T>GCA344585189LAMB3c.2792A>C (p.Lys931Thr)
c.-2A>C (n.-2A>C)
c.2600A>C (p.Lys867Thr)
1g.209618570T>ACA344585190LAMB3c.2791A>T (p.Lys931Ter)
c.-3A>T (n.-3A>T)
c.2599A>T (p.Lys867Ter)
1g.209618570T>CCA344585191LAMB3c.2791A>G (p.Lys931Glu)
c.-3A>G (n.-3A>G)
c.2599A>G (p.Lys867Glu)
dbSNP
1g.209618570T>GCA344585192LAMB3c.2791A>C (p.Lys931Gln)
c.-3A>C (n.-3A>C)
c.2599A>C (p.Lys867Gln)
1g.209618570T=CA2484296297LAMB3c.2791A= (p.Lys931=)
c.-3A= (n.-3A=)
c.2599A= (p.Lys867=)
1g.209618571C>ACA344585193LAMB3c.2790G>T (p.Gln930His)
c.-4G>T (n.-4G>T)
c.2598G>T (p.Gln866His)
1g.209618571C=CA2484296298LAMB3c.2790G= (p.Gln930=)
c.-4G= (n.-4G=)
c.2598G= (p.Gln866=)
1g.209618571C>GCA344585194LAMB3c.2790G>C (p.Gln930His)
c.-4G>C (n.-4G>C)
c.2598G>C (p.Gln866His)
1g.209618571C>TCA1375095LAMB3c.2790G>A (p.Gln930=)
c.-4G>A (n.-4G>A)
c.2598G>A (p.Gln866=)
dbSNP ExAC gnomAD v2 gnomAD v4
1g.209618572T>ACA344585195LAMB3c.2789A>T (p.Gln930Leu)
c.-5A>T (n.-5A>T)
c.2597A>T (p.Gln866Leu)
1g.209618572T>CCA344585196LAMB3c.2789A>G (p.Gln930Arg)
c.-5A>G (n.-5A>G)
c.2597A>G (p.Gln866Arg)
COSMIC
1g.209618572T>GCA344585197LAMB3c.2789A>C (p.Gln930Pro)
c.-5A>C (n.-5A>C)
c.2597A>C (p.Gln866Pro)
dbSNP
1g.209618572T=CA2484296299LAMB3c.2789A= (p.Gln930=)
c.-5A= (n.-5A=)
c.2597A= (p.Gln866=)
1g.209618573G>ACA344585198LAMB3c.2788C>T (p.Gln930Ter)
c.-6C>T (n.-6C>T)
c.2596C>T (p.Gln866Ter)
ClinVar dbSNP gnomAD v4
1g.209618573G>CCA344585199LAMB3c.2788C>G (p.Gln930Glu)
c.-6C>G (n.-6C>G)
c.2596C>G (p.Gln866Glu)
1g.209618573G>TCA344585200LAMB3c.2788C>A (p.Gln930Lys)
c.-6C>A (n.-6C>A)
c.2596C>A (p.Gln866Lys)
COSMIC
1g.209618574C>ACA423030108LAMB3c.2787G>T (p.Leu929=)
c.-7G>T (n.-7G>T)
c.2595G>T (p.Leu865=)
1g.209618574C>GCA423030109LAMB3c.2787G>C (p.Leu929=)
c.-7G>C (n.-7G>C)
c.2595G>C (p.Leu865=)
1g.209618574C>TCA423030110LAMB3c.2787G>A (p.Leu929=)
c.-7G>A (n.-7G>A)
c.2595G>A (p.Leu865=)
gnomAD v4
1g.209618575A>CCA344585201LAMB3c.2786T>G (p.Leu929Arg)
c.-8T>G (n.-8T>G)
c.2594T>G (p.Leu865Arg)
1g.209618575A>GCA344585203LAMB3c.2786T>C (p.Leu929Pro)
c.-8T>C (n.-8T>C)
c.2594T>C (p.Leu865Pro)
1g.209618575A>TCA344585202LAMB3c.2786T>A (p.Leu929Gln)
c.-8T>A (n.-8T>A)
c.2594T>A (p.Leu865Gln)
1g.209618576G>ACA423030114LAMB3c.2785C>T (p.Leu929=)
c.-9C>T (n.-9C>T)
c.2593C>T (p.Leu865=)
ClinVar dbSNP
1g.209618576G>CCA344585204LAMB3c.2785C>G (p.Leu929Val)
c.-9C>G (n.-9C>G)
c.2593C>G (p.Leu865Val)
1g.209618576G>TCA344585205LAMB3c.2785C>A (p.Leu929Met)
c.-9C>A (n.-9C>A)
c.2593C>A (p.Leu865Met)
1g.209618577A>CCA423030115LAMB3c.2784T>G (p.Val928=)
c.-10T>G (n.-10T>G)
c.2592T>G (p.Val864=)
1g.209618577A>GCA423030116LAMB3c.2784T>C (p.Val928=)
c.-10T>C (n.-10T>C)
c.2592T>C (p.Val864=)
1g.209618577A>TCA423030117LAMB3c.2784T>A (p.Val928=)
c.-10T>A (n.-10T>A)
c.2592T>A (p.Val864=)
1g.209618578A>CCA344585206LAMB3c.2783T>G (p.Val928Gly)
c.-11T>G (n.-11T>G)
c.2591T>G (p.Val864Gly)
1g.209618578A>GCA344585207LAMB3c.2783T>C (p.Val928Ala)
c.-11T>C (n.-11T>C)
c.2591T>C (p.Val864Ala)
gnomAD v4
1g.209618578A>TCA344585208LAMB3c.2783T>A (p.Val928Asp)
c.-11T>A (n.-11T>A)
c.2591T>A (p.Val864Asp)
1g.209618579C>ACA344585210LAMB3c.2782G>T (p.Val928Phe)
c.-12G>T (n.-12G>T)
c.2590G>T (p.Val864Phe)
1g.209618579C=CA2484296300LAMB3c.2782G= (p.Val928=)
c.-12G= (n.-12G=)
c.2590G= (p.Val864=)
1g.209618579C>GCA344585211LAMB3c.2782G>C (p.Val928Leu)
c.-12G>C (n.-12G>C)
c.2590G>C (p.Val864Leu)
dbSNP gnomAD v2 gnomAD v4
1g.209618579C>TCA344585209LAMB3c.2782G>A (p.Val928Ile)
c.-12G>A (n.-12G>A)
c.2590G>A (p.Val864Ile)
dbSNP gnomAD v2 gnomAD v4
1g.209618580A=CA2484296301LAMB3c.2781T= (p.Thr927=)
c.-13T= (n.-13T=)
c.2589T= (p.Thr863=)
1g.209618580A>CCA36750229LAMB3c.2781T>G (p.Thr927=)
c.-13T>G (n.-13T>G)
c.2589T>G (p.Thr863=)
dbSNP
1g.209618580A>GCA423030120LAMB3c.2781T>C (p.Thr927=)
c.-13T>C (n.-13T>C)
c.2589T>C (p.Thr863=)
1g.209618580A>TCA423030121LAMB3c.2781T>A (p.Thr927=)
c.-13T>A (n.-13T>A)
c.2589T>A (p.Thr863=)
1g.209618581G>ACA344585212LAMB3c.2780C>T (p.Thr927Ile)
c.-14C>T (n.-14C>T)
c.2588C>T (p.Thr863Ile)
1g.209618581G>CCA344585213LAMB3c.2780C>G (p.Thr927Ser)
c.-14C>G (n.-14C>G)
c.2588C>G (p.Thr863Ser)
1g.209618581G>TCA344585214LAMB3c.2780C>A (p.Thr927Asn)
c.-14C>A (n.-14C>A)
c.2588C>A (p.Thr863Asn)
1g.209618582T>ACA344585215LAMB3c.2779A>T (p.Thr927Ser)
c.-15A>T (n.-15A>T)
c.2587A>T (p.Thr863Ser)
1g.209618582T>CCA1375096LAMB3c.2779A>G (p.Thr927Ala)
c.-15A>G (n.-15A>G)
c.2587A>G (p.Thr863Ala)
dbSNP ExAC gnomAD v2 gnomAD v4
1g.209618582T>GCA344585216LAMB3c.2779A>C (p.Thr927Pro)
c.-15A>C (n.-15A>C)
c.2587A>C (p.Thr863Pro)
1g.209618582T=CA2484296302LAMB3c.2779A= (p.Thr927=)
c.-15A= (n.-15A=)
c.2587A= (p.Thr863=)
1g.209618583A>CCA423030123LAMB3c.2778T>G (p.Ala926=)
c.-16T>G (n.-16T>G)
c.2586T>G (p.Ala862=)
1g.209618583A>GCA423030124LAMB3c.2778T>C (p.Ala926=)
c.-16T>C (n.-16T>C)
c.2586T>C (p.Ala862=)
ClinVar

Number of alleles fetched