Variant #0000568518 (NC_000019.9:g.55669004G>A, NM_000363.4:c.-47C>T (TNNI3))

Chromosome 19
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.55669004G>A
DNA change (hg38) g.55157636G>A
Published as -
ISCN -
DB-ID TNNI3_000038 See all 2 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.0069 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TNNI3 NM_000363.4 -/. - c.-47C>T r.(?) p.(=)
DNAAF3 NM_001256715.1 -/. - c.*1426C>T r.(=) p.(=)
DNAAF3 NM_178837.4 -/. - c.*1426C>T r.(=) p.(=)


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