Variant #0001030077 (NC_000019.9:g.55665463G>A, NM_000363.4:c.484C>T (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.55665463G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID TNNI3_000013 See all 10 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs368861241
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 4.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-03-27 11:12:01 +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.484C>T r.(?) p.(Arg162Trp)


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