Variant (rsID / SNP)

rs139625465

rs139625465 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TIMM44. Location: chromosome 19, position 7,997,576. The table records no clinical significance for this variant.

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Reference-table entries

TIMM44Not classified

Variant type: single nucleotide variant
Chromosome / position: 19:7997576
Cytoband: 19p13.2
HGVS: NM_006351.4(TIMM44):c.923C>A (p.Pro308Gln)
Allele change: Missense_P308Q

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.