Variant #0000094929 (NC_000002.11:g.179391878T>G, NM_001267550.1:c.107837A>C (TTN))

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.179391878T>G
DNA change (hg38) g.178527151T>G
Published as H56P (H66P)
ISCN -
DB-ID TTN_000567 See all 4 reported entries
Variant remarks expression cloning in E.coli, biophysical in vitro characterization shows normal folding room T but unfolding at 37oC rendering it binding incompetent
Reference PubMed: Rudloff 2015, Journal: Rudloff 2015
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2016-04-19 10:57:28 +02:00 (CEST)
Date last edited 2020-07-14 21:50:58 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TTN NM_001267550.1 +/. 364 c.107837A>C r.(?) p.His35946Pro


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