Variant (rsID / SNP)

rs142817656

rs142817656 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TPM3. Location: chromosome 1, position 154,143,165. Clinical significance in the table: Uncertain significance.

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Reference-table entries

TPM3Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 1:154143165
Cytoband: 1q21.3
HGVS: NM_152263.4(TPM3):c.665A>T (p.Tyr222Phe)
Allele change: Silent

Associated conditions / phenotypes

Nemaline myopathy 1|Congenital myopathy with fiber type disproportion

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.