Variant #0000016946 (NC_000002.11:g.179391925_179391935delinsTTTTTCTTTCA, NM_001267550.1:c.107780_107790delinsTGAAAGAAAAA (TTN))

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.179391925_179391935delinsTTTTTCTTTCA
DNA change (hg38) g.178527198_178527208delinsTTTTTCTTTCA
Published as AJ277892: 293268-293280 AAGTAACATGG>TGAAAGAAAAA
ISCN -
DB-ID TTN_000004 See all 12 reported entries
Variant remarks Finnish major/founder TMD mutation, 12 Finnish TMD families; not in 216 controls (Finnish)
Reference PubMed: Hackman 2002
ClinVar ID -
dbSNP ID rs281864927
Origin SUMMARY record
Segregation yes
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Anne Polvi
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Anne Polvi
Date created 2012-12-17 12:40:55 +01:00 (CET)
Date last edited 2017-05-05 19:04:32 +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.107780_107790delinsTGAAAGAAAAA r.(?) p.(Glu35927_Trp35930delinsValLysGluLys)


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