Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 3:37048955 (forward strand) | View in location tab

Co-located

with COSMIC COSM1422604 (G/A) ; HGMD-PUBLIC CM960974 ; PhenCode MMR_c.2041G>A (G/A)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 1284, MLH1_complex_21

This variation has 19 HGVS names - click the plus to show

3:g.37048955G>A
ENST00000455445.4:c.1318G>A
ENSP00000398272.2:p.Ala440Thr
ENST00000413740.1:c.291-1531G>A
ENST00000231790.4:c.2041G>A
ENSP00000231790.2:p.Ala681Thr
ENST00000456676.4:c.1871+1272G>A
ENST00000539477.3:c.1318G>A
ENSP00000443665.1:p.Ala440Thr
ENST00000458205.4:c.1318G>A
ENSP00000402667.2:p.Ala440Thr
ENST00000435176.3:c.1747G>A
ENSP00000402564.1:p.Ala583Thr
ENST00000536378.3:c.1318G>A
ENSP00000444286.2:p.Ala440Thr
ENST00000450420.3:c.182-1531G>A
LRG_216:g.60606G>A
LRG_216t1:c.2041G>A
LRG_216p1:p.Ala681Thr

Variation displays