Variant #0000311938 (NC_000019.9:g.55665410C>T, NM_000363.4:c.537G>A (TNNI3))

Chromosome 19
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.55665410C>T
DNA change (hg38) g.55154042C>T
Published as TNNI3(NM_000363.4):c.537G>A (p.E179=), TNNI3(NM_000363.5):c.537G>A (p.E179=)
ISCN -
DB-ID TNNI3_000015 See all 6 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) 0.06528 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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.537G>A r.(?) p.(Glu179=)
DNAAF3 NM_001256715.1 -/. - c.*5020G>A r.(=) p.(=)
TNNT1 NM_003283.4 -/. - c.-4893G>A r.(?) p.(=)
DNAAF3 NM_178837.4 -/. - c.*5020G>A r.(=) p.(=)


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