Variant #0000288686 (NC_000016.9:g.57688016_57688022del, NM_005682.5:c.739_745del (GPR56))
Chromosome |
16 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.57688016_57688022del |
DNA change (hg38) |
g.57654104_57654110del |
Published as |
GPR56(NM_005682.6):c.739_745delCAGGACC (p.Q247Cfs*74) |
ISCN |
- |
DB-ID |
GPR56_000013 See all 2 reported entries |
Variant remarks |
VKGL data sharing initiative Nederland |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
CLASSIFICATION record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2018-01-15 20:58:59 +01:00 (CET) |
Date last edited |
2020-07-09 16:52:05 +02:00 (CEST) |

Variant on transcripts
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