Variant (rsID / SNP)

rs10410169

rs10410169 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MUC16. Location: chromosome 19, position 9,047,267. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

MUC16Not classified

Variant type: missense_variant
Chromosome / position: 19:9047267
HGVS: NM_001401501.1,c.34484G>A,p.Gly11495Asp
Allele change: Missense_G11455D

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.