Variant (rsID / SNP)

rs25497

rs25497 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TUBB. Location: chromosome 6, position 30,691,490. Clinical significance in the table: Benign.

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Reference-table entries

TUBBBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 6:30691490
Cytoband: 6p21.33
HGVS: NM_178014.4(TUBB):c.651G>A (p.Leu217=)
Allele change: Synonymous_L217L

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.