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 | MAF: 0.39 (T)
Location

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

Most severe consequence
Evidence status

This variation has 3 synonyms - click the plus to show

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

6:g.166165782C>T
ENST00000461348.2:c.530G>A
ENSP00000453512.1:p.Gly177Asp
ENST00000366871.5:c.530G>A
ENSP00000355836.3:p.Gly177Asp
ENST00000366876.4:c.530G>A
ENSP00000355841.2:p.Gly177Asp
ENST00000296946.4:c.530G>A
ENSP00000296946.2:p.Gly177Asp

This variation has assays on 10 chips - click the plus to show

Variation displays