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Variant (rsID / SNP)

rs7117111

CUL5

rs7117111 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CUL5. Location: chromosome 11, position 107,917,087. The table records no clinical significance for this variant.

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Reference-table entries

CUL5Not classified
Variant type
synonymous_variant
Chromosome / position
11:107917087
HGVS
NM_003478.6,c.225A>G,p.Gln75Gln
Allele change
Synonymous_Q75Q

Public references

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