Original source

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

A/C/G | Ancestral: A | Ambiguity code: V

Chromosome 16:176745 (forward strand) | View in location tab


with HGMD-PUBLIC CM086364 ; PhenCode HbVar.2594 (A/G) ; dbSNP rs35836455 (A/C)

Most severe consequence

This variation has 2 synonyms - click the plus to show

This variation has 10 HGVS names - click the plus to show

About this variant

This variant overlaps 21 transcripts.

Variation displays