Variant (rsID / SNP)

rs1129659

rs1129659 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NKAIN4. Location: chromosome 20, position 61,880,169. The table records no clinical significance for this variant.

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Reference-table entries

NKAIN4Not classified

Variant type: missense_variant&splice_region_variant
Chromosome / position: 20:61880169
HGVS: NM_152864.4,c.271A>C,p.Lys91Gln
Allele change: Missense_K29Q

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.