Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.6003688A>CCA153247769PMS2c.353+2T>G (p.=)
c.-53+2T>G (p.=)
n.35+284T>G (p.=)
n.432+2T>G
n.353+2T>G (p.=)
n.353+2T>G
n.546T>G
c.35+284T>G (p.=)
n.62+2305T>G
n.435+2T>G
c.347+2T>G (p.=)
c.398+2T>G (p.=)
c.-532+2T>G (p.=)
c.-132+2T>G (p.=)
n.440+2T>G
c.-432+2T>G (p.=)
dbSNP
7g.6003688A>GCA049344PMS2c.353+2T>C (p.=)
c.-53+2T>C (p.=)
n.35+284T>C (p.=)
n.432+2T>C
n.353+2T>C (p.=)
n.353+2T>C
n.546T>C
c.35+284T>C (p.=)
n.62+2305T>C
n.435+2T>C
c.347+2T>C (p.=)
c.398+2T>C (p.=)
c.-532+2T>C (p.=)
c.-132+2T>C (p.=)
n.440+2T>C
c.-432+2T>C (p.=)
ClinVar dbSNP ExAC gnomAD

Number of alleles fetched