Variant (rsID / SNP)

rs2547063

rs2547063 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MUC16. Location: chromosome 19, position 9,062,544. The table records no clinical significance for this variant.

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Reference-table entries

MUC16Not classified

Variant type: missense_variant
Chromosome / position: 19:9062544
HGVS: NM_001401501.1,c.25022A>C,p.Asn8341Thr
Allele change: Missense_N8301T

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.