Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
C/T|Ancestral: C|Ambiguity code: Y
Location

Chromosome 14:99718118 (forward strand)|View in location tab

Co-located variant

COSMIC COSM949257

Most severe consequence
 
Synonymous variant
Evidence status

Clinical significance

Synonyms

LSDB NC_000014.7:g.99254208C>T

HGVS names

This variant has 10 HGVS names - Show

About this variant

This variant overlaps 7 transcripts.

Variant displays