Variant #0000961145 (NC_000001.10:g.74701787T>A, NM_015978.2:c.42T>A (TNNI3K))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.74701787T>A
DNA change (hg38) -
Published as TNNI3K(NM_015978.3):c.42T>A (p.D14E)
ISCN -
DB-ID FPGT-TNNI3K_000165
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) 1.0E-5 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2024-02-26 20:06:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FPGT-TNNI3K NM_001112808.2 ?/. - c.384T>A r.(?) p.(Asp128Glu)
TNNI3K NM_015978.2 ?/. - c.42T>A r.(?) p.(Asp14Glu)


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