Variant #0000568470 (NC_000019.9:g.55665408T>C, NM_000363.4:c.539A>G (TNNI3))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.55665408T>C
DNA change (hg38) g.55154040T>C
Published as TNNI3(NM_000363.4):c.539A>G (p.D180G), TNNI3(NM_000363.5):c.539A>G (p.D180G)
ISCN -
DB-ID TNNI3_000062 See all 7 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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +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.539A>G r.(?) p.(Asp180Gly)
DNAAF3 NM_001256715.1 +?/. - c.*5022A>G r.(=) p.(=)
TNNT1 NM_003283.4 +?/. - c.-4891A>G r.(?) p.(=)
DNAAF3 NM_178837.4 +?/. - c.*5022A>G r.(=) p.(=)


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