Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

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

Chromosome 4:145639422 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM043524

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 14928, 2010_April_001_041_MMAA_607481_0003

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

4:g.145639422C>T
ENST00000506919.1:n.771C>T
ENST00000281317.7:c.283C>T
ENSP00000281317.5:p.Gln95Ter
ENST00000511969.2:c.283C>T
ENSP00000427422.1:p.Gln95Ter
ENST00000541599.3:c.283C>T
ENSP00000442284.2:p.Gln95Ter

Variation displays