Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.112838953G>CCA16028692APCc.3024G>C (n.3024G>C)
c.3413G>C (p.Gly1138Ala)
c.*3365G>C (n.*3365G>C)
c.3305G>C (p.Gly1102Ala)
c.3359G>C (p.Gly1120Ala)
c.1712G>C
c.*2681G>C (n.*2681G>C)
c.230+9981G>C
c.3389G>C (p.Gly1130Ala)
c.3284G>C (p.Gly1095Ala)
c.3275G>C (p.Gly1092Ala)
c.3236G>C (p.Gly1079Ala)
c.3182G>C (p.Gly1061Ala)
c.3086G>C (p.Gly1029Ala)
c.3056G>C (p.Gly1019Ala)
c.2981G>C (p.Gly994Ala)
c.2879G>C (p.Gly960Ala)
c.2510G>C (p.Gly837Ala)
 dbSNP COSMIC
5g.112838953G>ACA008319APCc.3024G>A (n.3024G>A)
c.3413G>A (p.Gly1138Glu)
c.*3365G>A (n.*3365G>A)
c.3305G>A (p.Gly1102Glu)
c.3359G>A (p.Gly1120Glu)
c.1712G>A
c.*2681G>A (n.*2681G>A)
c.230+9981G>A
c.3389G>A (p.Gly1130Glu)
c.3284G>A (p.Gly1095Glu)
c.3275G>A (p.Gly1092Glu)
c.3236G>A (p.Gly1079Glu)
c.3182G>A (p.Gly1061Glu)
c.3086G>A (p.Gly1029Glu)
c.3056G>A (p.Gly1019Glu)
c.2981G>A (p.Gly994Glu)
c.2879G>A (p.Gly960Glu)
c.2510G>A (p.Gly837Glu)
 ClinVar dbSNP COSMIC
5g.112838953G>TCA16028693APCc.3024G>T (n.3024G>T)
c.3413G>T (p.Gly1138Val)
c.*3365G>T (n.*3365G>T)
c.3305G>T (p.Gly1102Val)
c.3359G>T (p.Gly1120Val)
c.1712G>T
c.*2681G>T (n.*2681G>T)
c.230+9981G>T
c.3389G>T (p.Gly1130Val)
c.3284G>T (p.Gly1095Val)
c.3275G>T (p.Gly1092Val)
c.3236G>T (p.Gly1079Val)
c.3182G>T (p.Gly1061Val)
c.3086G>T (p.Gly1029Val)
c.3056G>T (p.Gly1019Val)
c.2981G>T (p.Gly994Val)
c.2879G>T (p.Gly960Val)
c.2510G>T (p.Gly837Val)
 dbSNP

Number of alleles fetched