Variant #0000799513 (NC_000001.10:g.74818986A>G, NM_015978.2:c.969A>G (TNNI3K))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.74818986A>G
DNA change (hg38) -
Published as FPGT-TNNI3K(NM_001112808.3):c.1272A>G (p.K424=), TNNI3K(NM_015978.2):c.969A>G (p.K323=), TNNI3K(NM_015978.3):c.969A>G (p.K323=)
ISCN -
DB-ID FPGT-TNNI3K_000024 See all 3 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) 0.00108 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +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.1311A>G r.(?) p.(Lys437=)
TNNI3K NM_015978.2 -?/. - c.969A>G r.(?) p.(Lys323=)


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