Variant (rsID / SNP)
rs1292053
rs1292053 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TUBD1. Location: chromosome 17, position 57,963,537. The table records no clinical significance for this variant.
Reference-table entries
TUBD1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 17:57963537
- HGVS
- NM_016261.4,c.227T>C,p.Met76Thr
- Allele change
- Silent
Associated conditions / phenotypes
Missense_M76T
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.