Variant (rsID / SNP)

rs183134138

rs183134138 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MTMR14. Location: chromosome 3, position 9,726,588. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

MTMR14Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 3:9726588
Cytoband: 3p25.3
HGVS: NM_001077525.3(MTMR14):c.1067C>T (p.Thr356Met)
Allele change: Missense_T356M

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.