Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R
Location

Chromosome 4:145646043 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM043528

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_042_MMAA_607481_0004, 14929

This variation has 9 HGVS names - click the plus to show

4:g.145646043A>G
ENST00000506919.1:n.1108A>G
ENST00000281317.7:c.620A>G
ENSP00000281317.5:p.Tyr207Cys
ENST00000511969.2:c.620A>G
ENSP00000427422.1:p.Tyr207Cys
ENST00000541599.3:c.620A>G
ENSP00000442284.2:p.Tyr207Cys
ENST00000504555.1:n.254-3216T>C

Variation displays