Variant (rsID / SNP)

rs148433331

rs148433331 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRIM63. Location: chromosome 1, position 26,387,763. Clinical significance in the table: Uncertain significance.

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Reference-table entries

TRIM63Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 1:26387763
Cytoband: 1p36.11
HGVS: NM_032588.4(TRIM63):c.395T>C (p.Ile132Thr)
Allele change: Missense_I132T

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.