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 InternationalCreative Commons License
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)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GPR56 NM_005682.5 +/. - c.739_745del r.(?) p.(Gln247CysfsTer74)


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