Variant #0000562737 (NC_000017.10:g.63221579C>T, NM_003835.3:c.1867C>T (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.63221579C>T
DNA change (hg38) g.65225461C>T
Published as RGS9(NM_003835.3):c.1867C>T (p.R623*), RGS9(NM_003835.4):c.1867C>T (p.R623*)
ISCN -
DB-ID RGS9_000022 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) 5.0E-5 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RGS9 NM_001165933.1 ?/. - c.*14799C>T r.(=) p.(=)
RGS9 NM_003835.3 ?/. - c.1867C>T r.(?) p.(Arg623Ter)


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