Variant #0000446998 (NC_000001.10:g.154164469A>C, NM_152263.3:c.26T>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.154164469A>C
DNA change (hg38) g.154191993A>C
Published as -
ISCN -
DB-ID TPM3_000001 See all 7 reported entries
Variant remarks adenovirus transduced rat cardiac myocytes, incorporated correctly, decreased sensitivity contraction, no direct nemaline rod formation
Reference PubMed: Michele 1999, OMIM:var0001
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2008-09-22 10:14:28 +02:00 (CEST)
Date last edited 2020-07-14 21:57:48 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TPM3 NM_152263.3 +/. 1 c.26T>G r.(?) p.Met9Arg


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