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Variant (rsID / SNP)

rs138085432

MMUT

rs138085432 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MMUT. Location: chromosome 6, position 49,425,446. Clinical significance in the table: Benign.

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Reference-table entries

MMUTBenign
Clinical significance (as recorded)
Benign
Variant type
single nucleotide variant
Chromosome / position
6:49425446
Cytoband
6p12.3
HGVS
NM_000255.4(MMUT):c.711A>G (p.Pro237=)
Allele change
Synonymous_P237P

Associated conditions / phenotypes

Methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency|Methylmalonic aciduria due to complete methylmalonyl-CoA mutase deficiency

Public references

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