This variation has been flagged

None of the variant alleles match the reference allele (A)

Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/G/T | Ancestral: A | Ambiguity code: B
Note: The reference base for this variant (C) does not match the Ensembl reference base (A) at this location.
Location

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

Co-located

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

Most severe consequence

This variation has 2 synonyms - click the plus to show

This variation has 14 HGVS names - click the plus to show

About this variant

This variant overlaps 31 transcripts.

Variation displays