Variant (rsID / SNP)

rs1128864

rs1128864 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ART3. Location: chromosome 4, position 77,033,590. The table records no clinical significance for this variant.

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Reference-table entries

ART3Not classified

Variant type: missense_variant
Chromosome / position: 4:77033590
HGVS: NM_001377173.1,c.1121C>T,p.Ser374Leu
Allele change: Missense_S341L

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.