Variant #0000562733 (NC_000017.10:g.63204074A>G, NM_003835.3:c.1238A>G (RGS9))

Chromosome 17
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.63204074A>G
DNA change (hg38) g.65207956A>G
Published as -
ISCN -
DB-ID RGS9_000020
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 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-05-09 15:24:52 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RGS9 NM_001165933.1 ?/. - c.1229A>G r.(?) p.(Tyr410Cys)
RGS9 NM_003835.3 ?/. - c.1238A>G r.(?) p.(Tyr413Cys)


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