Variant #0000969994 (NC_000019.9:g.55665589G>C, NC_000019.9(NM_000363.4):c.373-15C>G (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.55665589G>C
DNA change (hg38) -
Published as TNNI3(NM_000363.4):c.373-15C>G, TNNI3(NM_000363.5):c.373-15C>G
ISCN -
DB-ID DNAAF3_000024 See all 3 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) 0.00029 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2024-02-26 20:06:56 +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.373-15C>G r.(=) p.(=)
DNAAF3 NM_001256715.1 -?/. - c.*4841C>G r.(=) p.(=)
TNNT1 NM_003283.4 -?/. - c.-5072C>G r.(?) p.(=)
DNAAF3 NM_178837.4 -?/. - c.*4841C>G r.(=) p.(=)


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