Variant #0000558481 (NC_000016.9:g.56226508C>A, NM_020988.2:c.141C>A (GNAO1))

Chromosome 16
Allele Unknown
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.56226508C>A
DNA change (hg38) g.56192596C>A
Published as GNAO1(NM_138736.3):c.141C>A (p.S47R)
ISCN -
DB-ID GNAO1_000022 See all 3 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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-10-19 14:52:41 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GNAO1 NM_020988.2 +?/. - c.141C>A r.(?) p.(Ser47Arg)
GNAO1 NM_138736.2 +?/. - c.141C>A r.(?) p.(Ser47Arg)


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