Variant (rsID / SNP)

rs145471785

rs145471785 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TENT5C. Location: chromosome 1, position 118,166,385. The table records no clinical significance for this variant.

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Reference-table entries

TENT5CNot classified

Variant type: single nucleotide variant
Chromosome / position: 1:118166385
Cytoband: 1p12
HGVS: NM_017709.4(TENT5C):c.895G>A (p.Glu299Lys)
Allele change: Missense_E299K

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.