Variant #0000924969 (NC_000009.11:g.131763869C>T, NM_015354.2:c.3905C>T (NUP188))

Chromosome 9
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.131763869C>T
DNA change (hg38) -
Published as NUP188(NM_015354.3):c.3905C>T (p.S1302F)
ISCN -
DB-ID DOLK_000020
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 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DOLK NM_014908.3 ?/. - c.-54287G>A r.(?) p.(=)
NUP188 NM_015354.2 ?/. - c.3905C>T r.(?) p.(Ser1302Phe)


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