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Variant (rsID / SNP)

rs80162610

CCDC158

rs80162610 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCDC158. Location: chromosome 4, position 77,305,566. The table records no clinical significance for this variant.

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Reference-table entries

CCDC158Not classified
Variant type
missense_variant&splice_region_variant
Chromosome / position
4:77305566
HGVS
NM_001394954.1,c.401G>A,p.Arg134Gln
Allele change
Missense_R134Q

Public references

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