Variant #0000097159 (NC_000006.11:g.(24291307_24301943)_(24302074_24302195)del, DCDC2(NM_016356.3):c.(425+1_426-1)_(557+1_558-1)del)
Individual ID |
00065308 |
Chromosome |
6 |
Allele |
Both (homozygous) |
Affects function (as reported) |
Probably affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.(24291307_24301943)_(24302074_24302195)del |
DNA change (hg38) |
- |
Published as |
- |
ISCN |
- |
DB-ID |
DCDC2_000000 |
Variant remarks |
- |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Germline |
Segregation |
yes |
Frequency |
- |
Re-site |
- |
VIP |
0 |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Variant not found in online data sets |
Owner |
Muriel Girard |
Database submission license |
No license selected |
Created by |
Muriel Girard |

Variant on transcripts
Screenings
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