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 International |
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) |

Variant on transcripts
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