Variant #0000294832 (NC_000017.10:g.63154436G>A, NM_003835.3:c.178G>A (RGS9))

Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.63154436G>A
DNA change (hg38) g.65158318G>A
Published as RGS9(NM_003835.3):c.178G>A (p.V60I), RGS9(NM_003835.4):c.178G>A (p.V60I)
ISCN -
DB-ID RGS9_000001 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) 0.00104 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 2018-01-15 20:58:59 +01:00 (CET)
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.178G>A r.(?) p.(Val60Ile)
RGS9 NM_003835.3 -/. - c.178G>A r.(?) p.(Val60Ile)


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