Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.37008813G>TCA010579MLH1c.454-1G>T (p.=)
c.-270-1G>T (p.=)
c.*534-1G>T (p.=)
n.469-1G>T
c.91-1G>T (p.=)
c.-179+1750G>T (p.=)
n.407-1G>T
n.485-1G>T
c.*246-1G>T (p.=)
c.*594-1G>T (p.=)
c.*332-1G>T (p.=)
n.439-1G>T
n.396-1G>T
c.160-1G>T (p.=)
c.*327-1G>T (p.=)
n.429-1G>T
c.*233-1G>T (p.=)
n.487-1G>T
n.458-1G>T
n.477-1G>T
c.-476-1G>T (p.=)
c.-373-1G>T (p.=)
c.-363-1G>T (p.=)
c.-282+1750G>T (p.=)
c.355-1G>T (p.=)
ClinVar dbSNP
3g.37008813G>ACA010570MLH1c.454-1G>A (p.=)
c.-270-1G>A (p.=)
c.*534-1G>A (p.=)
n.469-1G>A
c.91-1G>A (p.=)
c.-179+1750G>A (p.=)
n.407-1G>A
n.485-1G>A
c.*246-1G>A (p.=)
c.*594-1G>A (p.=)
c.*332-1G>A (p.=)
n.439-1G>A
n.396-1G>A
c.160-1G>A (p.=)
c.*327-1G>A (p.=)
n.429-1G>A
c.*233-1G>A (p.=)
n.487-1G>A
n.458-1G>A
n.477-1G>A
c.-476-1G>A (p.=)
c.-373-1G>A (p.=)
c.-363-1G>A (p.=)
c.-282+1750G>A (p.=)
c.355-1G>A (p.=)
ClinVar dbSNP
3g.37008813G>CCA16042068MLH1c.454-1G>C (p.=)
c.-270-1G>C (p.=)
c.*534-1G>C (p.=)
n.469-1G>C
c.91-1G>C (p.=)
c.-179+1750G>C (p.=)
n.407-1G>C
n.485-1G>C
c.*246-1G>C (p.=)
c.*594-1G>C (p.=)
c.*332-1G>C (p.=)
n.439-1G>C
n.396-1G>C
c.160-1G>C (p.=)
c.*327-1G>C (p.=)
n.429-1G>C
c.*233-1G>C (p.=)
n.487-1G>C
n.458-1G>C
n.477-1G>C
c.-476-1G>C (p.=)
c.-373-1G>C (p.=)
c.-363-1G>C (p.=)
c.-282+1750G>C (p.=)
c.355-1G>C (p.=)
ClinVar dbSNP

Number of alleles fetched