Variant #0000658665 (NC_000019.9:g.55665438C>T, NM_000363.4:c.509G>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.55665438C>T
DNA change (hg38) g.55154070C>T
Published as TNNI3(NM_000363.4):c.509G>A (p.R170Q)
ISCN -
DB-ID TNNI3_000056 See all 6 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) Retrieve
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +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 +/. - c.509G>A r.(?) p.(Arg170Gln)
DNAAF3 NM_001256715.1 +/. - c.*4992G>A r.(=) p.(=)
TNNT1 NM_003283.4 +/. - c.-4921G>A r.(?) p.(=)
DNAAF3 NM_178837.4 +/. - c.*4992G>A r.(=) p.(=)


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