Variant #0000307067 (NC_000019.9:g.33167295G>C, NM_207391.2:c.126G>C (RGS9BP))

Chromosome 19
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.33167295G>C
DNA change (hg38) g.32676389G>C
Published as RGS9BP(NM_207391.2):c.126G>C (p.K42N), RGS9BP(NM_207391.3):c.126G>C (p.K42N)
ISCN -
DB-ID RGS9BP_000002 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) 0.00028 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NUDT19 NM_001105570.1 ?/. - c.-15572G>C r.(?) p.(=)
ANKRD27 NM_032139.2 ?/. - c.-1349C>G r.(?) p.(=)
RGS9BP NM_207391.2 ?/. - c.126G>C r.(?) p.(Lys42Asn)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.