Variant #0000536467 (NC_000009.11:g.131767814T>G, NC_000009.11(NM_015354.2):c.4737+5T>G (NUP188))

Chromosome 9
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.131767814T>G
DNA change (hg38) g.129005535T>G
Published as NUP188(NM_015354.1):c.4737+5T>G (p.?)
ISCN -
DB-ID DOLK_000012
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DOLK NM_014908.3 -?/. - c.-58232A>C r.(?) p.(=)
NUP188 NM_015354.2 -?/. - c.4737+5T>G r.spl? p.?
SH3GLB2 NM_020145.2 -?/. - c.*3149A>C r.(=) p.(=)


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