Variant #0000558482 (NC_000016.9:g.56226536C>T, NC_000016.9(NM_020988.2):c.161+8C>T (GNAO1))

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.56226536C>T
DNA change (hg38) g.56192624C>T
Published as GNAO1(NM_020988.3):c.161+8C>T
ISCN -
DB-ID GNAO1_000023
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) 0.00169 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-11-27 17:27:23 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GNAO1 NM_020988.2 -?/. - c.161+8C>T r.(=) p.(=)
GNAO1 NM_138736.2 -?/. - c.161+8C>T r.(=) p.(=)


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