Variant #0000016952 (NC_000002.11:g.179391878T>G, NM_001267550.1:c.107837A>C (TTN))

Chromosome 2
Allele Parent #1
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.179391878T>G
DNA change (hg38) g.178527151T>G
Published as AJ277892:g.293326A>C (H33378P)
ISCN -
DB-ID TTN_000567 See all 4 reported entries
Variant remarks Italian TMD family (het)
Reference PubMed: Pollazzon 2010
ClinVar ID -
dbSNP ID rs281864931
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 13:38:33 +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.107837A>C r.(?) p.(His35946Pro)


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