Variant #0000275160 (NC_000019.9:g.55670651C>T, NM_000363.4:c.-1694G>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.55670651C>T
DNA change (hg38) g.55159283C>T
Published as DNAAF3(NM_001256714.1):c.1606G>A (p.V536M), DNAAF3(NM_001256715.2):c.1405G>A (p.(Val469Met))
ISCN -
DB-ID DNAAF3_000002 See all 2 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) 0.00212 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 2018-01-15 20:58:59 +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.-1694G>A r.(?) p.(=)
DNAAF3 NM_001256715.1 -?/. - c.1405G>A r.(?) p.(Val469Met)
DNAAF3 NM_178837.4 -?/. - c.1546G>A r.(?) p.(Val516Met)


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