Variant #0001061191 (NC_000001.10:g.154164487T>C, NM_152263.3:c.8A>G (TPM3))

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.154164487T>C
DNA change (hg38) g.154192011T>C
Published as -
ISCN -
DB-ID TPM3_000053 See all 5 reported entries
Variant remarks biochemical in vitro assays revealed defects in assembly thin filament and regulation of actin–myosin interactions
Reference PubMed: Robaszkiewicz 2023
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Joanna Moraczewska
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2025-12-12 16:15:16 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TPM3 NM_152263.3 +/. - c.8A>G - p.Glu3Gly


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