Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.39 (T)
Location

Chromosome 6:166165782 (forward strand)|View in location tab

Most severe consequence
 
Missense variant
Evidence status

Synonyms

This variant has 3 synonyms - Show

HGVS names

This variant has 9 HGVS names - Hide

6:g.166165782C>T
ENST00000366876.6:c.530G>A
ENSP00000355841.2:p.Gly177Asp
ENST00000296946.6:c.530G>A
ENSP00000296946.2:p.Gly177Asp
ENST00000461348.2:c.530G>A
ENSP00000453512.1:p.Gly177Asp
ENST00000366871.7:c.530G>A
ENSP00000355836.3:p.Gly177Asp

Genotyping chips

This variant has assays on 11 chips - Show

About this variant

This variant overlaps 4 transcripts, 1 regulatory feature, has 3984 sample genotypes and is mentioned in 7 citations.

Variant displays