Variant #0000617888 (NC_000019.9:g.55670642C>T, NM_000363.4:c.-1685G>A (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.55670642C>T
DNA change (hg38) g.55159274C>T
Published as -
ISCN -
DB-ID DNAAF3_000061
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) 0.00037 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.-1685G>A r.(?) p.(=)
DNAAF3 NM_001256715.1 -?/. - c.1414G>A r.(?) p.(Gly472Arg)
DNAAF3 NM_178837.4 -?/. - c.1555G>A r.(?) p.(Gly519Arg)


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