Variant #0000566826 (NC_000019.9:g.33167641G>A, NM_207391.2:c.472G>A (RGS9BP))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.33167641G>A
DNA change (hg38) g.32676735G>A
Published as RGS9BP(NM_207391.2):c.472G>A (p.G158S)
ISCN -
DB-ID ANKRD27_000007
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +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.-15226G>A r.(?) p.(=)
ANKRD27 NM_032139.2 -?/. - c.-1695C>T r.(?) p.(=)
RGS9BP NM_207391.2 -?/. - c.472G>A r.(?) p.(Gly158Ser)


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