Variant #0000000690 (NC_000002.11:g.179401179C>T, NM_001267550.1:c.100295G>A (TTN))

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg19 / GRCh37) g.179401179C>T
Reference -
DB-ID TTN_000009
Frequency -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2025-10-06 08:32:54 +00:00 (UTC)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Class     
TTN NM_001267550.1 ?/? - c.100295G>A r.? p.(Arg33432His) VUS
TTN NM_133379.4 ?/? - c.*209133G>A r.? p.? VUS