Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.36996617A>GCA004620MLH1c.117-2A>G (p.=)
c.-173-2A>G (p.=)
c.-602-7A>G (p.=)
c.-515-2A>G (p.=)
c.-517+2954A>G (p.=)
c.-752-2A>G (p.=)
c.-607-2A>G (p.=)
c.-813-2A>G (p.=)
c.-710-2A>G (p.=)
c.-510-2A>G (p.=)
c.-510-7A>G (p.=)
c.-168-7A>G (p.=)
c.-700-2A>G (p.=)
c.-723+2727A>G (p.=)
c.-608-7A>G (p.=)
c.-705-7A>G (p.=)
c.-695-7A>G (p.=)
c.*197-2A>G (p.=)
c.116+2954A>G (p.=)
c.117-7A>G (p.=)
n.92-2A>G
n.44-2A>G
n.239-2A>G
n.121-2A>G
n.140-2A>G
ClinVar dbSNP
3g.36996617A>TCA72786559MLH1c.117-2A>T (p.=)
c.-173-2A>T (p.=)
c.-602-7A>T (p.=)
c.-515-2A>T (p.=)
c.-517+2954A>T (p.=)
c.-752-2A>T (p.=)
c.-607-2A>T (p.=)
c.-813-2A>T (p.=)
c.-710-2A>T (p.=)
c.-510-2A>T (p.=)
c.-510-7A>T (p.=)
c.-168-7A>T (p.=)
c.-700-2A>T (p.=)
c.-723+2727A>T (p.=)
c.-608-7A>T (p.=)
c.-705-7A>T (p.=)
c.-695-7A>T (p.=)
c.*197-2A>T (p.=)
c.116+2954A>T (p.=)
c.117-7A>T (p.=)
n.92-2A>T
n.44-2A>T
n.239-2A>T
n.121-2A>T
n.140-2A>T
dbSNP COSMIC

Number of alleles fetched