Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.116782027G>TCA256994METc.*1167G>T (n.*1167G>T)
c.3616G>T (p.Val1206Leu)
c.3562G>T (p.Val1188Leu)
c.2272G>T (p.Val758Leu)
c.3619G>T (p.Val1207Leu)
n.3693G>T
ClinVar dbSNP COSMIC
7g.116782027G>ACA4448748METc.*1167G>A (n.*1167G>A)
c.3616G>A (p.Val1206Ile)
c.3562G>A (p.Val1188Ile)
c.2272G>A (p.Val758Ile)
c.3619G>A (p.Val1207Ile)
n.3693G>A
ClinVar dbSNP ExAC gnomAD v2
7g.116782027G>CCA368990990METc.*1167G>C (n.*1167G>C)
c.3616G>C (p.Val1206Leu)
c.3562G>C (p.Val1188Leu)
c.2272G>C (p.Val758Leu)
c.3619G>C (p.Val1207Leu)
n.3693G>C
dbSNP COSMIC

Number of alleles fetched