Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.16 (C)
Location

Chromosome 16:31357553 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58681810, rs56622927

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

16:g.31357553T>C
ENST00000268296.6:c.430+189T>C
ENST00000562522.2:c.430+189T>C
ENST00000562918.3:c.538T>C
ENSP00000483860.1:p.Phe180Leu
ENST00000567409.1:n.837T>C

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

Variation displays