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Variant (rsID / SNP)

rs116114439

TAF1B

rs116114439 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TAF1B. Location: chromosome 2, position 10,045,113. The table records no clinical significance for this variant.

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Reference-table entries

TAF1BNot classified
Variant type
synonymous_variant
Chromosome / position
2:10045113
HGVS
NM_005680.3,c.933C>T,p.Tyr311Tyr
Allele change
Synonymous_Y56Y

Public references

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