Variant #0000983665 (NC_000019.9:g.55673132_55673133dup, NM_000363.4:c.-4174_-4173dup (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.55673132_55673133dup
DNA change (hg38) -
Published as DNAAF3(NM_001256715.2):c.543_544dup (p.(Gln182Profs*6))
ISCN -
DB-ID DNAAF3_000094
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +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.-4174_-4173dup r.(?) p.(=)
DNAAF3 NM_001256715.1 ?/. - c.543_544dup r.(?) p.(Gln182Profs*6)
DNAAF3 NM_178837.4 ?/. - c.684_685dup r.(?) p.(Gln229Profs*6)


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