Variant #0000355099 (NC_000019.9:g.55665463G>A, NM_000363.4:c.484C>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.55665463G>A
DNA change (hg38) g.55154095G>A
Published as -
ISCN -
DB-ID TNNI3_000013 See all 9 reported entries
Variant remarks -
Reference {PMID10806205:Elliott 2000}
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 4.0E-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 2011-08-01 11:40:36 +02:00 (CEST)
Date last edited 2020-07-16 13:59:33 +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 ?/. 7 c.484C>T r.(?) p.Arg162Trp


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