Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.209617526C>ACA344584184LAMB3c.3112G>T (p.Asp1038Tyr)
c.319G>T (p.Asp107Tyr)
c.2920G>T (p.Asp974Tyr)
1g.209617526C=CA2484295891LAMB3c.3112G= (p.Asp1038=)
c.319G= (p.Asp107=)
c.2920G= (p.Asp974=)
1g.209617526C>GCA344584186LAMB3c.3112G>C (p.Asp1038His)
c.319G>C (p.Asp107His)
c.2920G>C (p.Asp974His)
1g.209617526C>TCA344584188LAMB3c.3112G>A (p.Asp1038Asn)
c.319G>A (p.Asp107Asn)
c.2920G>A (p.Asp974Asn)
 dbSNP
1g.209617527A>CCA423029554LAMB3c.3111T>G (p.Gly1037=)
c.318T>G (p.Gly106=)
c.2919T>G (p.Gly973=)
1g.209617527A>GCA423029555LAMB3c.3111T>C (p.Gly1037=)
c.318T>C (p.Gly106=)
c.2919T>C (p.Gly973=)
 ClinVar
1g.209617527A>TCA423029556LAMB3c.3111T>A (p.Gly1037=)
c.318T>A (p.Gly106=)
c.2919T>A (p.Gly973=)
 gnomAD v4
1g.209617528C>ACA344584195LAMB3c.3110G>T (p.Gly1037Val)
c.317G>T (p.Gly106Val)
c.2918G>T (p.Gly973Val)
1g.209617528C>GCA344584191LAMB3c.3110G>C (p.Gly1037Ala)
c.317G>C (p.Gly106Ala)
c.2918G>C (p.Gly973Ala)
1g.209617528C>TCA344584193LAMB3c.3110G>A (p.Gly1037Asp)
c.317G>A (p.Gly106Asp)
c.2918G>A (p.Gly973Asp)
 gnomAD v4
1g.209617529C>ACA344584199LAMB3c.3109G>T (p.Gly1037Cys)
c.316G>T (p.Gly106Cys)
c.2917G>T (p.Gly973Cys)
1g.209617529C>GCA344584201LAMB3c.3109G>C (p.Gly1037Arg)
c.316G>C (p.Gly106Arg)
c.2917G>C (p.Gly973Arg)
1g.209617529C>TCA344584203LAMB3c.3109G>A (p.Gly1037Ser)
c.316G>A (p.Gly106Ser)
c.2917G>A (p.Gly973Ser)
1g.209617530C>ACA423029560LAMB3c.3108G>T (p.Leu1036=)
c.315G>T (p.Leu105=)
c.2916G>T (p.Leu972=)
 gnomAD v4
1g.209617530C>GCA423029559LAMB3c.3108G>C (p.Leu1036=)
c.315G>C (p.Leu105=)
c.2916G>C (p.Leu972=)
1g.209617530C>TCA423029558LAMB3c.3108G>A (p.Leu1036=)
c.315G>A (p.Leu105=)
c.2916G>A (p.Leu972=)
1g.209617531A>CCA344584205LAMB3c.3107T>G (p.Leu1036Arg)
c.314T>G (p.Leu105Arg)
c.2915T>G (p.Leu972Arg)
1g.209617531A>GCA344584207LAMB3c.3107T>C (p.Leu1036Pro)
c.314T>C (p.Leu105Pro)
c.2915T>C (p.Leu972Pro)
1g.209617531A>TCA344584209LAMB3c.3107T>A (p.Leu1036Gln)
c.314T>A (p.Leu105Gln)
c.2915T>A (p.Leu972Gln)
1g.209617532G>ACA423029563LAMB3c.3106C>T (p.Leu1036=)
c.313C>T (p.Leu105=)
c.2914C>T (p.Leu972=)
1g.209617532G>CCA344584211LAMB3c.3106C>G (p.Leu1036Val)
c.313C>G (p.Leu105Val)
c.2914C>G (p.Leu972Val)
1g.209617532G>TCA344584213LAMB3c.3106C>A (p.Leu1036Met)
c.313C>A (p.Leu105Met)
c.2914C>A (p.Leu972Met)
1g.209617533C>ACA344584215LAMB3c.3105G>T (p.Gln1035His)
c.312G>T (p.Gln104His)
c.2913G>T (p.Gln971His)
1g.209617533C>GCA344584217LAMB3c.3105G>C (p.Gln1035His)
c.312G>C (p.Gln104His)
c.2913G>C (p.Gln971His)
1g.209617533C>TCA423029566LAMB3c.3105G>A (p.Gln1035=)
c.312G>A (p.Gln104=)
c.2913G>A (p.Gln971=)
1g.209617534T>ACA344584219LAMB3c.3104A>T (p.Gln1035Leu)
c.311A>T (p.Gln104Leu)
c.2912A>T (p.Gln971Leu)
1g.209617534T>CCA344584221LAMB3c.3104A>G (p.Gln1035Arg)
c.311A>G (p.Gln104Arg)
c.2912A>G (p.Gln971Arg)
1g.209617534T>GCA344584222LAMB3c.3104A>C (p.Gln1035Pro)
c.311A>C (p.Gln104Pro)
c.2912A>C (p.Gln971Pro)
 gnomAD v4
1g.209617535G>ACA344584228LAMB3c.3103C>T (p.Gln1035Ter)
c.310C>T (p.Gln104Ter)
c.2911C>T (p.Gln971Ter)
 gnomAD v4
1g.209617535G>CCA344584225LAMB3c.3103C>G (p.Gln1035Glu)
c.310C>G (p.Gln104Glu)
c.2911C>G (p.Gln971Glu)
1g.209617535G>TCA344584227LAMB3c.3103C>A (p.Gln1035Lys)
c.310C>A (p.Gln104Lys)
c.2911C>A (p.Gln971Lys)
1g.209617536C>ACA344584229LAMB3c.3102G>T (p.Lys1034Asn)
c.309G>T (p.Lys103Asn)
c.2910G>T (p.Lys970Asn)
1g.209617536C>GCA344584230LAMB3c.3102G>C (p.Lys1034Asn)
c.309G>C (p.Lys103Asn)
c.2910G>C (p.Lys970Asn)
1g.209617536C>TCA423029567LAMB3c.3102G>A (p.Lys1034=)
c.309G>A (p.Lys103=)
c.2910G>A (p.Lys970=)
 ClinVar gnomAD v4
1g.209617537T>ACA344584232LAMB3c.3101A>T (p.Lys1034Met)
c.308A>T (p.Lys103Met)
c.2909A>T (p.Lys970Met)
1g.209617537T>CCA344584234LAMB3c.3101A>G (p.Lys1034Arg)
c.308A>G (p.Lys103Arg)
c.2909A>G (p.Lys970Arg)
1g.209617537T>GCA344584236LAMB3c.3101A>C (p.Lys1034Thr)
c.308A>C (p.Lys103Thr)
c.2909A>C (p.Lys970Thr)
1g.209617538T>ACA344584242LAMB3c.3100A>T (p.Lys1034Ter)
c.307A>T (p.Lys103Ter)
c.2908A>T (p.Lys970Ter)
1g.209617538T>CCA344584240LAMB3c.3100A>G (p.Lys1034Glu)
c.307A>G (p.Lys103Glu)
c.2908A>G (p.Lys970Glu)
1g.209617538T>GCA344584238LAMB3c.3100A>C (p.Lys1034Gln)
c.307A>C (p.Lys103Gln)
c.2908A>C (p.Lys970Gln)
1g.209617539G>ACA423029568LAMB3c.3099C>T (p.Thr1033=)
c.306C>T (p.Thr102=)
c.2907C>T (p.Thr969=)
1g.209617539G>CCA423029569LAMB3c.3099C>G (p.Thr1033=)
c.306C>G (p.Thr102=)
c.2907C>G (p.Thr969=)
 ClinVar dbSNP
1g.209617539G>TCA423029571LAMB3c.3099C>A (p.Thr1033=)
c.306C>A (p.Thr102=)
c.2907C>A (p.Thr969=)
1g.209617540G>ACA344584251LAMB3c.3098C>T (p.Thr1033Ile)
c.305C>T (p.Thr102Ile)
c.2906C>T (p.Thr969Ile)
 dbSNP gnomAD v4
1g.209617540G>CCA344584253LAMB3c.3098C>G (p.Thr1033Ser)
c.305C>G (p.Thr102Ser)
c.2906C>G (p.Thr969Ser)
1g.209617540G>TCA344584255LAMB3c.3098C>A (p.Thr1033Asn)
c.305C>A (p.Thr102Asn)
c.2906C>A (p.Thr969Asn)
 gnomAD v4
1g.209617541T>ACA344584256LAMB3c.3097A>T (p.Thr1033Ser)
c.304A>T (p.Thr102Ser)
c.2905A>T (p.Thr969Ser)
1g.209617541T>CCA344584258LAMB3c.3097A>G (p.Thr1033Ala)
c.304A>G (p.Thr102Ala)
c.2905A>G (p.Thr969Ala)
1g.209617541T>GCA344584260LAMB3c.3097A>C (p.Thr1033Pro)
c.304A>C (p.Thr102Pro)
c.2905A>C (p.Thr969Pro)
1g.209617542C>ACA344584263LAMB3c.3096G>T (p.Met1032Ile)
c.303G>T (p.Met101Ile)
c.2904G>T (p.Met968Ile)

Number of alleles fetched