Original source

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

Alleles
T/A | Ancestral: T | Ambiguity code: W
Location

Chromosome 5:36953698 (forward strand) | View in location tab

Co-located

with COSMIC COSM1739176 (T/A), COSM1739175 (T/A) ; HGMD-PUBLIC CM041503

Most severe consequence
Clinical significance

Synonyms

LSDB 15878

This variation has 6 HGVS names - click the plus to show

5:g.36953698T>A
ENST00000448238.2:c.2T>A
ENSP00000406266.2:p.Met1?
ENST00000282516.10:c.2T>A
ENSP00000282516.8:p.Met1?
ENST00000621733.1:c.-1+76676T>A

Variation displays