Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

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

Chromosome 12:33031955 (forward strand) | View in location tab

Co-located

with COSMIC COSM468293 (G/A) ; HGMD-PUBLIC CM043053

Most severe consequence
Clinical significance

Synonyms

LSDB 11517

This variation has 5 HGVS names - click the plus to show

12:g.33031955G>A
ENST00000340811.4:c.235C>T
ENSP00000342800.4:p.Arg79Ter
ENST00000070846.6:c.235C>T
ENSP00000070846.6:p.Arg79Ter

Variation displays