Variant (rsID / SNP)
rs642215
rs642215 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TMPRSS4. Location: chromosome 11, position 117,988,082. The table records no clinical significance for this variant.
Reference-table entries
TMPRSS4Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 11:117988082
- HGVS
- NM_019894.4,c.1215T>C,p.Ser405Ser
- Allele change
- Synonymous_S405S
Associated conditions / phenotypes
Silent|Synonymous_S258S
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.