Variant #0000324805 (NC_000016.9:g.57685534A>C, NM_005682.5:c.487A>C (GPR56))

Chromosome 16
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.57685534A>C
DNA change (hg38) g.57651622A>C
Published as ADGRG1(NM_001145772.2):c.487A>C (p.S163R), GPR56(NM_001145770.1):c.487A>C (p.?)
ISCN -
DB-ID GPR56_000006 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) 1.0E-5 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 2018-01-15 20:58:59 +01:00 (CET)
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.487A>C r.(?) p.(Ser163Arg)


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