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Variant (rsID / SNP)

rs13016342

NCKAP5

rs13016342 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NCKAP5. Location: chromosome 2, position 133,540,605. The table records no clinical significance for this variant.

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Reference-table entries

NCKAP5Not classified
Variant type
missense_variant
Chromosome / position
2:133540605
HGVS
NM_207363.3,c.3779C>A,p.Pro1260Gln
Allele change
Silent

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.