Variant #0000508294 (NC_000001.10:g.74701895G>A, NC_000001.10(NM_015978.2):c.149+1G>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.74701895G>A
DNA change (hg38) g.74236211G>A
Published as TNNI3K(NM_015978.3):c.149+1G>A
ISCN -
DB-ID FPGT-TNNI3K_000006
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FPGT-TNNI3K NM_001112808.2 ?/. - c.491+1G>A r.spl? p.?
TNNI3K NM_015978.2 ?/. - c.149+1G>A r.spl? p.?


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