Variant #0000536466 (NC_000009.11:g.131765218G>A, NM_015354.2:c.4260G>A (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.131765218G>A
DNA change (hg38) g.129002939G>A
Published as NUP188(NM_015354.2):c.4260G>A (p.L1420=)
ISCN -
DB-ID DOLK_000011
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) 0.00011 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DOLK NM_014908.3 -?/. - c.-55636C>T r.(?) p.(=)
NUP188 NM_015354.2 -?/. - c.4260G>A r.(?) p.(Leu1420=)
SH3GLB2 NM_020145.2 -?/. - c.*5745C>T r.(=) p.(=)


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