Variant #0000275155 (NC_000019.9:g.55672129G>A, NM_000363.4:c.-3172C>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.55672129G>A
DNA change (hg38) g.55160761G>A
Published as DNAAF3(NM_001256714.1):c.1131C>T (p.I377=)
ISCN -
DB-ID DNAAF3_000009
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 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.-3172C>T r.(?) p.(=)
DNAAF3 NM_001256715.1 -?/. - c.927C>T r.(?) p.(Ile309=)
DNAAF3 NM_178837.4 -?/. - c.1068C>T r.(?) p.(Ile356=)


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