Variant (rsID / SNP)
rs34080891
rs34080891 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TUBAL3. Location: chromosome 10, position 5,436,073. The table records no clinical significance for this variant.
Reference-table entries
TUBAL3Not classified
- Variant type
- missense_variant
- Chromosome / position
- 10:5436073
- HGVS
- NM_024803.3,c.748C>T,p.Arg250Trp
- Allele change
- Missense_R210W
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
