Variant (rsID / SNP)
rs3739407
rs3739407 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MTUS1. Location: chromosome 8, position 17,612,875. The table records no clinical significance for this variant.
Reference-table entries
MTUS1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 8:17612875
- HGVS
- NM_001363057.2,c.442T>C,p.Cys148Arg
- Allele change
- Missense_C148R
Associated conditions / phenotypes
Missense_C148R|Missense_C148R|Missense_C148R|Missense_C148R
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.