Variant #0000983663 (NC_000019.9:g.55672494G>T, NM_000363.4:c.-3537C>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.55672494G>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID DNAAF3_000093
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) 1.0E-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 2024-04-19 20:27:30 +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.-3537C>A r.(?) p.(=)
DNAAF3 NM_001256715.1 ?/. - c.851C>A r.(?) p.(Ala284Asp)
DNAAF3 NM_178837.4 ?/. - c.992C>A r.(?) p.(Ala331Asp)


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