Variant #0000078699 (NC_000015.9:g.41221866_41230233=, NM_019074.3:c.-1_*1= (DLL4))
Individual ID |
00049874 |
Chromosome |
15 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.41221866_41230233= |
DNA change (hg38) |
- |
Published as |
- |
ISCN |
- |
DB-ID |
DLL4_000000 |
Variant remarks |
no variant detected in blood sample Variant Error [EMISMATCH/EREF]: This transcript variant does not match the reference sequence. Please fix this entry and then remove this message. |
Reference |
PubMed: Meester 2015, Journal: Meester 2015 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Unknown |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Johan den Dunnen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |
Date created |
2015-09-13 21:13:34 +02:00 (CEST) |
Date last edited |
N/A |

Variant on transcripts
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