Variant #0000558614 (NC_000016.9:g.57691409G>A, NC_000016.9(NM_005682.5):c.1286+6G>A (GPR56))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.57691409G>A
DNA change (hg38) g.57657497G>A
Published as GPR56(NM_001145770.1):c.1286+6G>A (p.(=)), GPR56(NM_005682.6):c.1286+6G>A
ISCN -
DB-ID GPR56_000023 See all 4 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) 0.02392 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2019-12-04 15:24:38 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GPR56 NM_005682.5 -?/. - c.1286+6G>A r.(=) p.(=)


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