Variant #0000297665 (NC_000019.9:g.33167879G>A, NM_207391.2:c.*2G>A (RGS9BP))

Chromosome 19
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.33167879G>A
DNA change (hg38) g.32676973G>A
Published as RGS9BP(NM_207391.3):c.*2G>A
ISCN -
DB-ID RGS9BP_000009
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) 0.60265 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NUDT19 NM_001105570.1 -/. - c.-14988G>A r.(?) p.(=)
ANKRD27 NM_032139.2 -/. - c.-1933C>T r.(?) p.(=)
RGS9BP NM_207391.2 -/. - c.*2G>A r.(=) p.(=)


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