Variant (rsID / SNP)

rs1041316

rs1041316 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TMEM260. Location: chromosome 14, position 57,099,859. The table records no clinical significance for this variant.

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Reference-table entries

TMEM260Not classified

Variant type: missense_variant
Chromosome / position: 14:57099859
HGVS: NM_017799.4,c.1694G>A,p.Ser565Asn
Allele change: Missense_S565N

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.