Variant #0000971556 (NC_000019.9:g.55663278C>T, NM_000363.4:c.557G>A (TNNI3))

Chromosome 19
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.55663278C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID TNNI3_000032 See all 9 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs397516357
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2024-03-07 08:57:02 +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     
TNNI3 NM_000363.4 +/. - c.557G>A r.(?) p.(Arg186Gln)


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