Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

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

Chromosome 4:146567195 (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 8 HGVS names - click the plus to show

4:g.146567195A>G
ENST00000506919.1:n.1108A>G
ENST00000281317.5:c.620A>G
ENSP00000281317.5:p.Tyr207Cys
ENST00000511969.1:c.620A>G
ENSP00000427422.1:p.Tyr207Cys
ENST00000541599.1:c.-138A>G
ENST00000504555.1:n.254-3216T>C

Variation displays