Variant #0000355105 (NC_000019.9:g.55668953G>A, NM_000363.4:c.5C>T (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.55668953G>A
DNA change (hg38) g.55157585G>A
Published as 4C>T
ISCN -
DB-ID TNNI3_000039 See all 4 reported entries
Variant remarks -
Reference {PMID15070570:Murphy 2004}
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 3.0E-5 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2013-12-28 10:24:14 +01:00 (CET)
Date last edited 2020-07-16 14:07:33 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TNNI3 NM_000363.4 ?/. 1 c.5C>T r.(?) p.(Ala2Val)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.