Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: < 0.01 (T)
Location

Chromosome 2:71895914 (forward strand) | View in location tab

Co-located

with COSMIC COSM107021 (C/T)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NC_000002.10:g.71749422C>T

This variation has 24 HGVS names - click the plus to show

Somatic mutation displays