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: 0.12 (T)
Location

Chromosome 16:31325567 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 5 synonyms - click the plus to show

This variation has 6 HGVS names - click the plus to show

16:g.31325567C>T
ENST00000287497.9:c.2573C>T
ENSP00000287497.8:p.Ala858Val
ENST00000561838.1:n.389C>T
ENST00000544665.4:c.2576C>T
ENSP00000441691.2:p.Ala859Val

This variation has assays on 13 chips - click the plus to show

Variation displays