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 14:100184455 (forward strand) | View in location tab

Co-located

with COSMIC COSM949257 (C/T)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NC_000014.7:g.99254208C>T

This variation has 8 HGVS names - click the plus to show

Variation displays