Variant #0000000475 (NC_000002.11:g.179634392A>T, NC_000002.11(NM_001267550.1):c.8902+14T>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.179634392A>T
Reference -
DB-ID TTN_000008
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 2024-05-03 08:40:54 +00:00 (UTC)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TTN NM_001267550.1 ?/? - c.8902+14T>A r.(=) p.(=)
TTN NM_133379.4 ?/? - c.8902+14T>A r.(=) p.(=)