Variant (rsID / SNP)

rs149544914

rs149544914 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SYT14. Location: chromosome 1, position 210,273,523. Clinical significance in the table: Uncertain significance.

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Reference-table entries

SYT14Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 1:210273523
Cytoband: 1q32.2
HGVS: NM_001146262.4(SYT14):c.881G>A (p.Gly294Asp)
Allele change: Missense_G256D

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.