Variant (rsID / SNP)

rs2277369

rs2277369 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CALCOCO1. Location: chromosome 12, position 54,110,197. The table records no clinical significance for this variant.

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Reference-table entries

CALCOCO1Not classified

Variant type: splice_region_variant&synonymous_variant
Chromosome / position: 12:54110197
HGVS: NM_020898.3,c.852T>C,p.Ala284Ala
Allele change: Silent

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.