Variant (rsID / SNP)
rs7099565
rs7099565 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRUB1. Location: chromosome 10, position 116,719,543. The table records no clinical significance for this variant.
Reference-table entries
TRUB1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 10:116719543
- HGVS
- NM_139169.5,c.500G>A,p.Arg167Lys
- Allele change
- Missense_R167K
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.