Variant #0000508300 (NC_000001.10:g.74797154A>G, NM_015978.2:c.465A>G (TNNI3K))

Chromosome 1
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.74797154A>G
DNA change (hg38) g.74331470A>G
Published as FPGT-TNNI3K(NM_001112808.3):c.768A>G (p.Q256=), TNNI3K(NM_015978.2):c.465A>G (p.Q155=), TNNI3K(NM_015978.3):c.465A>G (p.Q155=)
ISCN -
DB-ID FPGT-TNNI3K_000011 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) 0.00026 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 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.807A>G r.(?) p.(Gln269=)
TNNI3K NM_015978.2 -/. - c.465A>G r.(?) p.(Gln155=)


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