Variant (rsID / SNP)

rs791323

rs791323 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TUT7. Location: chromosome 9, position 88,959,938. The table records no clinical significance for this variant.

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Reference-table entries

TUT7Not classified

Variant type: synonymous_variant
Chromosome / position: 9:88959938
HGVS: NM_001185059.2,c.951G>A,p.Leu317Leu
Allele change: Synonymous_L317L

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.