Variant #0000000126 (NC_000002.11:g.179612667G>T, TTN(NM_001267550.1):c.11311+5184C>A)

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg19 / GRCh37) g.179612667G>T
Reference -
DB-ID TTN_000001 See all 2 reported entries
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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TTN NM_001267550.1 ?/? - c.11311+5184C>A r.(=) p.(=)
TTN NM_133379.4 ?/? 46 c.14460C>A r.(?) p.(Asp4820Glu)