Variant (rsID / SNP)

rs12540688

rs12540688 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NUP205. Location: chromosome 7, position 135,329,690. The table records no clinical significance for this variant.

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Reference-table entries

NUP205Not classified

Variant type: synonymous_variant
Chromosome / position: 7:135329690
HGVS: NM_015135.3,c.5607T>C,p.Ala1869Ala
Allele change: Synonymous_A1869A

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.