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 14:94849249 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM971177

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 33032, NP_000286.3:p.THR85MET

This variation has 29 HGVS names - click the plus to show

Variation displays