Variant (rsID / SNP)

rs140262959

rs140262959 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MTIF3. Location: chromosome 13, position 28,014,173. Clinical significance in the table: Likely benign.

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Reference-table entries

MTIF3Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 13:28014173
Cytoband: 13q12.2
HGVS: NM_152912.5(MTIF3):c.413A>G (p.Gln138Arg)
Allele change: Missense_Q138R

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.