Variant #0000016949 (NC_000002.11:g.179392206del, NM_001267550.1:c.107647del (TTN))

Chromosome 2
Allele Paternal (confirmed)
Affects function (as reported) Affects function
Affects function (by curator) Probably affects function
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.179392206del
DNA change (hg38) g.178527479del
Published as AJ277892.2:g.292998delT (S33315QfsX10)
ISCN -
DB-ID TTN_000041 See all 3 reported entries
Variant remarks French TMD family (het)
Reference PubMed: Hackman 2008
ClinVar ID -
dbSNP ID rs281864932
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 13:24:51 +01:00 (CET)
Date last edited 2020-06-10 09:21:29 +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 +/+? 363 c.107647del r.(?) p.(Ser35883Glnfs*10)


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