Variant #0001046664 (NC_000017.10:g.63193278T>C, NM_003835.3:c.895T>C (RGS9))

Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.63193278T>C
DNA change (hg38) -
Published as RGS9(NM_003835.4):c.895T>C (p.W299R, p.(Trp299Arg))
ISCN -
DB-ID RGS9_000012 See all 6 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) 0.00011 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2025-07-08 13:22:38 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RGS9 NM_001165933.1 +/. - c.886T>C r.(?) p.(Trp296Arg)
RGS9 NM_003835.3 +/. - c.895T>C r.(?) p.(Trp299Arg)


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