Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.116783421G>TCA16602657METc.*1355G>T (n.*1355G>T)
c.3804G>T (p.Met1268Ile)
c.3750G>T (p.Met1250Ile)
c.2460G>T (p.Met820Ile)
c.3807G>T (p.Met1269Ile)
n.3881G>T
ClinVar dbSNP
7g.116783421G>CCA16602656METc.*1355G>C (n.*1355G>C)
c.3804G>C (p.Met1268Ile)
c.3750G>C (p.Met1250Ile)
c.2460G>C (p.Met820Ile)
c.3807G>C (p.Met1269Ile)
n.3881G>C
ClinVar dbSNP
7g.116783421G>ACA123611METc.*1355G>A (n.*1355G>A)
c.3804G>A (p.Met1268Ile)
c.3750G>A (p.Met1250Ile)
c.2460G>A (p.Met820Ile)
c.3807G>A (p.Met1269Ile)
n.3881G>A
ClinVar dbSNP COSMIC

Number of alleles fetched