Variant (rsID / SNP)

rs10410136

rs10410136 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MUC16. Location: chromosome 19, position 9,056,941. The table records no clinical significance for this variant.

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Reference-table entries

MUC16Not classified

Variant type: missense_variant
Chromosome / position: 19:9056941
HGVS: NM_001401501.1,c.30625T>C,p.Phe10209Leu
Allele change: Missense_F10169L

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.