Variant #0000947293 (NC_000001.10:g.74737346G>T, NM_015978.2:c.398G>T (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.74737346G>T
DNA change (hg38) -
Published as TNNI3K(NM_015978.3):c.398G>T (p.G133V)
ISCN -
DB-ID FPGT-TNNI3K_000160
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) 7.0E-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 2023-11-27 17:35:39 +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.740G>T r.(?) p.(Gly247Val)
TNNI3K NM_015978.2 ?/. - c.398G>T r.(?) p.(Gly133Val)


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