Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/G/T | Ancestral: C | Ambiguity code: B
Location

Chromosome 12:25227346 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM061080, CM092327

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 5702, 5691, 2010_April_001_077_KRAS_190070_0009

This variation has 12 HGVS names - click the plus to show

About this variant

This variant overlaps 8 transcripts and is associated with 4 phenotypes.

Variation displays