Variant #0000568469 (NC_000019.9:g.55665404G>A, NM_000363.4:c.543C>T (TNNI3))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.55665404G>A
DNA change (hg38) g.55154036G>A
Published as TNNI3(NM_000363.4):c.543C>T (p.T181=), TNNI3(NM_000363.5):c.543C>T (p.T181=)
ISCN -
DB-ID TNNI3_000121 See all 3 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 2019-07-18 18:22:55 +02:00 (CEST)
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.543C>T r.(?) p.(Thr181=)
DNAAF3 NM_001256715.1 -?/. - c.*5026C>T r.(=) p.(=)
TNNT1 NM_003283.4 -?/. - c.-4887C>T r.(?) p.(=)
DNAAF3 NM_178837.4 -?/. - c.*5026C>T r.(=) p.(=)


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