Variant #0000355100 (NC_000019.9:g.55663260C>T, NM_000363.4:c.575G>A (TNNI3))

Chromosome 19
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.55663260C>T
DNA change (hg38) g.55151892C>T
Published as -
ISCN -
DB-ID TNNI3_000024 See all 4 reported entries
Variant remarks -
Reference {PMID15961398:Gomes 2005}
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 2011-08-02 10:19:14 +02:00 (CEST)
Date last edited 2020-07-16 13:56:46 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TNNI3 NM_000363.4 ?/. 8 c.575G>A r.(?) p.Arg192His


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