Variant #0000306706 (NC_000017.10:g.5212026T>A, NM_002532.4:c.*77500A>T (NUP88))

Chromosome 17
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.5212026T>A
DNA change (hg38) g.5308731T>A
Published as RABEP1(NM_004703.6):c.72T>A (p.I24=)
ISCN -
DB-ID RABEP1_000001
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-11 14:02:31 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NUP88 NM_002532.4 -?/. - c.*77500A>T r.(=) p.(=)
RABEP1 NM_004703.4 -?/. - c.72T>A r.(?) p.(Ile24=)


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