Variant (rsID / SNP)

rs1951716

rs1951716 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UNC79. Location: chromosome 14, position 94,007,075. The table records no clinical significance for this variant.

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Reference-table entries

UNC79Not classified

Variant type: synonymous_variant
Chromosome / position: 14:94007075
HGVS: NM_001395159.1,c.1422C>T,p.Gly474Gly
Allele change: Synonymous_G297G

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.