Variant #0000234999 (NC_000004.11:g.(107700001_114100000)_qterdelins[NC_000008.10:(118811950_119123286)_qter])
Individual ID |
00133224 |
Chromosome |
4 |
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.(107700001_114100000)_qterdelins[NC_000008.10:(118811950_119123286)_qter] |
DNA change (hg38) |
- |
Published as |
- |
ISCN |
t(4;8)(q25;q24.1) |
DB-ID |
chr4_000576 |
Variant remarks |
- |
Reference |
PubMed: Jennes, 2008 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Germline |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Genomic location of variant could not be determined |
Owner |
Ivy Jennes |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Johan den Dunnen |
Date created |
2017-12-01 19:40:26 +01:00 (CET) |
Date last edited |
2020-05-12 19:21:26 +02:00 (CEST) |
Variant on transcripts
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