Variant (rsID / SNP)

rs142238093

rs142238093 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TUBB3. Location: chromosome 16, position 90,002,146. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

TUBB3Conflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Chromosome / position: 16:90002146
Cytoband: 16q24.3
HGVS: NM_006086.4(TUBB3):c.1287G>A (p.Thr429=)
Allele change: Synonymous_T357T

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.