Variant #0000809056 (NC_000019.9:g.55670772G>A, NM_000363.4:c.-1815C>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.55670772G>A
DNA change (hg38) -
Published as DNAAF3(NM_001256716.1):c.1122C>T (p.T374=)
ISCN -
DB-ID DNAAF3_000072
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +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.-1815C>T r.(?) p.(=)
DNAAF3 NM_001256715.1 -?/. - c.1284C>T r.(?) p.(Thr428=)
DNAAF3 NM_178837.4 -?/. - c.1425C>T r.(?) p.(Thr475=)


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