Variant #0000566823 (NC_000019.9:g.33167446_33167447del, NM_207391.2:c.277_278del (RGS9BP))

Chromosome 19
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.33167446_33167447del
DNA change (hg38) g.32676540_32676541del
Published as RGS9BP(NM_207391.3):c.277_278delAT (p.M93Afs*206)
ISCN -
DB-ID ANKRD27_000004
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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.-15421_-15420del r.(?) p.(=)
ANKRD27 NM_032139.2 +/. - c.-1501_-1500del r.(?) p.(=)
RGS9BP NM_207391.2 +/. - c.277_278del r.(?) p.(Met93AlafsTer206)


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