Variant #0001032169 (NC_000001.10:g.74808631C>T, NM_015978.2:c.788C>T (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.74808631C>T
DNA change (hg38) -
Published as FPGT-TNNI3K(NM_001112808.2):c.1130C>T (p.P377L), FPGT-TNNI3K(NM_001112808.3):c.1091C>T (p.P364L), TNNI3K(NM_015978.2):c.788C>T (p.P263L), TNNI3K(N...)
ISCN -
DB-ID FPGT-TNNI3K_000018 See all 4 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) 0.00244 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
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.1130C>T r.(?) p.(Pro377Leu)
TNNI3K NM_015978.2 -/. - c.788C>T r.(?) p.(Pro263Leu)


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