Variant #0000560500 (NC_000017.10:g.17697214_17697229dup, NM_030665.3:c.952_967dup (RAI1))

Chromosome 17
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.17697214_17697229dup
DNA change (hg38) g.17793900_17793915dup
Published as RAI1(NM_030665.4):c.952_967dupGGCCAGGGCTACTGCC (p.Q323Rfs*71)
ISCN -
DB-ID RAI1_000098
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SREBF1 NM_004176.4 +/. - c.*18707_*18722dup r.(=) p.(=)
RAI1 NM_030665.3 +/. - c.952_967dup r.(?) p.(Gln323ArgfsTer71)


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