Variant #0000294836 (NC_000019.9:g.33167274C>T, NM_207391.2:c.105C>T (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.33167274C>T
DNA change (hg38) g.32676368C>T
Published as RGS9BP(NM_207391.3):c.105C>T (p.N35=)
ISCN -
DB-ID RGS9BP_000001
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) 0.0001 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     
NUDT19 NM_001105570.1 -/. - c.-15593C>T r.(?) p.(=)
ANKRD27 NM_032139.2 -/. - c.-1328G>A r.(?) p.(=)
RGS9BP NM_207391.2 -/. - c.105C>T r.(?) p.(Asn35=)


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