Variant (rsID / SNP)

rs1108380

rs1108380 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MUC16. Location: chromosome 19, position 9,085,958. 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: 19:9085958
HGVS: NM_001401501.1,c.5977T>C,p.Ser1993Pro
Allele change: Missense_S1953P

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.