Variant #0000000739 (NC_000002.11:g.179421854G>C, NM_001267550.1:c.88027C>G (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.179421854G>C
Reference -
DB-ID TTN_000010
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 2026-06-29 06:19:34 +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.88027C>G r.(?) p.(Arg29343Gly) VUS
TTN NM_133379.4 ?/? - c.*188458C>G r.(=) p.(=) VUS