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Variant (rsID / SNP)

rs140929639

KIF5A

rs140929639 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KIF5A. Location: chromosome 12, position 57,963,454. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

KIF5AConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
12:57963454
Cytoband
12q13.3
HGVS
NM_004984.4(KIF5A):c.1105C>T (p.Arg369Trp)
Allele change
Missense_R280W

Associated conditions / phenotypes

Spastic paraplegia|Hereditary spastic paraplegia 10|Hereditary spastic paraplegia

Public references

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