Variant #0000016950 (NC_000002.11:g.179391828del, NM_001267550.1:c.107889del (TTN))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.179391828del
DNA change (hg38) g.178527101del
Published as AJ277892.2:g.293378delA (K33395NfsX9)
ISCN -
DB-ID TTN_000042 See all 13 reported entries
Variant remarks 2 Spanish TMD families (het)
Reference PubMed: Hackman 2008
ClinVar ID -
dbSNP ID rs281864930
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 13:32:12 +01:00 (CET)
Date last edited 2020-06-10 09:18:15 +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.107889del r.(?) p.(Lys35963Asnfs*9)


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