Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.112837690G>CCA16025908APCc.1761G>C (n.1761G>C)
c.2150G>C (p.Trp717Ser)
c.*2102G>C (n.*2102G>C)
c.2042G>C (p.Trp681Ser)
c.2096G>C (p.Trp699Ser)
c.449G>C
c.785G>C (p.Trp262Ser)
c.*1418G>C (n.*1418G>C)
c.230+8718G>C
c.2126G>C (p.Trp709Ser)
c.2021G>C (p.Trp674Ser)
c.2012G>C (p.Trp671Ser)
c.1973G>C (p.Trp658Ser)
c.1919G>C (p.Trp640Ser)
c.1823G>C (p.Trp608Ser)
c.1793G>C (p.Trp598Ser)
c.1718G>C (p.Trp573Ser)
c.1616G>C (p.Trp539Ser)
c.1247G>C (p.Trp416Ser)
dbSNP
5g.112837690G>ACA16025907APCc.1761G>A (n.1761G>A)
c.2150G>A (p.Trp717Ter)
c.*2102G>A (n.*2102G>A)
c.2042G>A (p.Trp681Ter)
c.2096G>A (p.Trp699Ter)
c.449G>A
c.785G>A (p.Trp262Ter)
c.*1418G>A (n.*1418G>A)
c.230+8718G>A
c.2126G>A (p.Trp709Ter)
c.2021G>A (p.Trp674Ter)
c.2012G>A (p.Trp671Ter)
c.1973G>A (p.Trp658Ter)
c.1919G>A (p.Trp640Ter)
c.1823G>A (p.Trp608Ter)
c.1793G>A (p.Trp598Ter)
c.1718G>A (p.Trp573Ter)
c.1616G>A (p.Trp539Ter)
c.1247G>A (p.Trp416Ter)
ClinVar dbSNP
5g.112837690G>TCA16025909APCc.1761G>T (n.1761G>T)
c.2150G>T (p.Trp717Leu)
c.*2102G>T (n.*2102G>T)
c.2042G>T (p.Trp681Leu)
c.2096G>T (p.Trp699Leu)
c.449G>T
c.785G>T (p.Trp262Leu)
c.*1418G>T (n.*1418G>T)
c.230+8718G>T
c.2126G>T (p.Trp709Leu)
c.2021G>T (p.Trp674Leu)
c.2012G>T (p.Trp671Leu)
c.1973G>T (p.Trp658Leu)
c.1919G>T (p.Trp640Leu)
c.1823G>T (p.Trp608Leu)
c.1793G>T (p.Trp598Leu)
c.1718G>T (p.Trp573Leu)
c.1616G>T (p.Trp539Leu)
c.1247G>T (p.Trp416Leu)
dbSNP

Number of alleles fetched