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Variant (rsID / SNP)

rs183941928

TRIOBP

rs183941928 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRIOBP. Location: chromosome 22, position 38,153,696. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

TRIOBPBenign
Clinical significance (as recorded)
Benign/Likely benign
Variant type
single nucleotide variant
Chromosome / position
22:38153696
Cytoband
22q13.1
HGVS
NM_001039141.3(TRIOBP):c.5764C>T (p.Arg1922Trp)
Allele change
Missense_R1922W

Public references

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