Variant #0000335904 (NC_000023.10:g.150869303dup, NM_024082.3:c.494dup (PRRG3))

Chromosome X
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.150869303dup
DNA change (hg38) g.151700831dup
Published as PRRG3(NM_024082.3):c.487_488insG (p.(Arg166GlnfsTer14))
ISCN -
DB-ID PRRG3_000006
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-21 12:55:58 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRRG3 NM_024082.3 ?/. - c.494dup r.(?) p.(Arg166GlnfsTer14)


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