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 4:995875 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM960875

Most severe consequence
Clinical significance

Synonyms

LSDB 6457

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

4:g.995875G>A
ENST00000514224.1:c.502G>A
ENSP00000425081.1:p.Ala168Thr
ENST00000514698.1:n.898G>A
ENST00000453894.1:c.857G>A
ENSP00000396458.1:p.Gly286Asp
ENST00000247933.4:c.898G>A
ENSP00000247933.4:p.Ala300Thr

Variation displays