Variant (rsID / SNP)

rs61756351

rs61756351 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRAP1. Location: chromosome 16, position 3,716,025. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

TRAP1Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 16:3716025
Cytoband: 16p13.3
HGVS: NM_016292.3(TRAP1):c.1330T>A (p.Tyr444Asn)
Allele change: Missense_Y444N

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.