Variant (rsID / SNP)

rs79290430

rs79290430 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRIM36. Location: chromosome 5, position 114,469,808. The table records no clinical significance for this variant.

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Reference-table entries

TRIM36Not classified

Variant type: missense_variant
Chromosome / position: 5:114469808
HGVS: NM_018700.4,c.1283A>G,p.Lys428Arg
Allele change: Missense_K416R

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.