Variant (rsID / SNP)

rs12461007

rs12461007 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MUC16. Location: chromosome 19, position 9,049,149. The table records no clinical significance for this variant.

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Reference-table entries

MUC16Not classified

Variant type: missense_variant
Chromosome / position: 19:9049149
HGVS: NM_001401501.1,c.32602C>T,p.Pro10868Ser
Allele change: Missense_P10828S

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.