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Variant (rsID / SNP)

rs2288101

GALNT14

rs2288101 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GALNT14. Location: chromosome 2, position 31,135,184. The table records no clinical significance for this variant.

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Reference-table entries

GALNT14Not classified
Variant type
missense_variant
Chromosome / position
2:31135184
HGVS
NM_001253826.2,c.1420C>A,p.Gln474Lys
Allele change
Missense_Q474K

Associated conditions / phenotypes

Missense_Q434K

Public references

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