This variation has been flagged

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

Original source

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

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

Chromosome 22:23310360 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 2 synonyms - click the plus to show

This variation has 19 HGVS names - click the plus to show

Variation displays