Variant (rsID / SNP)
rs42663
rs42663 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GTPBP10. Location: chromosome 7, position 89,983,808. The table records no clinical significance for this variant.
Reference-table entries
GTPBP10Not classified
- Variant type
- missense_variant
- Chromosome / position
- 7:89983808
- HGVS
- NM_033107.4,c.264T>G,p.Cys88Trp
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.