This variation has been flagged

None of the variant alleles match the reference allele

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Original source

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

C/T | Ancestral: C | Ambiguity code: Y

This variation maps to 2 genomic locations; None selected

Clinical significance

This variation has 2 synonyms - click the plus to show

HGVS name


Variation displays