Variant #0000617876 (NC_000019.9:g.55665519G>T, NM_000363.4:c.428C>A (TNNI3))

Chromosome 19
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.55665519G>T
DNA change (hg38) g.55154151G>T
Published as TNNI3(NM_000363.5):c.428C>A (p.T143N)
ISCN -
DB-ID DNAAF3_000022 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) 4.0E-5 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 2019-12-04 15:24:38 +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.428C>A r.(?) p.(Thr143Asn)
DNAAF3 NM_001256715.1 ?/. - c.*4911C>A r.(=) p.(=)
TNNT1 NM_003283.4 ?/. - c.-5002C>A r.(?) p.(=)
DNAAF3 NM_178837.4 ?/. - c.*4911C>A r.(=) p.(=)


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