Variant #0000536456 (NC_000009.11:g.131708619G>A, NM_015354.2:c.-1380G>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.131708619G>A
DNA change (hg38) g.128946340G>A
Published as DOLK(NM_014908.3):c.964C>T (p.(Arg322Trp))
ISCN -
DB-ID DOLK_000004
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) 1.0E-5 View details
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)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DOLK NM_014908.3 -?/. - c.964C>T r.(?) p.(Arg322Trp)
NUP188 NM_015354.2 -?/. - c.-1380G>A r.(?) p.(=)
PHYHD1 NM_174933.3 -?/. - c.*4587G>A r.(=) p.(=)


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