Variant #0000522600 (NC_000004.11:g.44692845_44692848dup, NM_021927.2:c.1447_1450dup (GUF1))

Chromosome 4
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.44692845_44692848dup
DNA change (hg38) g.44690828_44690831dup
Published as GUF1(NM_021927.2):c.1447_1450dupGAAT (p.Y484*)
ISCN -
DB-ID GNPDA2_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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-16 12:54:39 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GUF1 NM_021927.2 +?/. - c.1447_1450dup r.(?) p.(Tyr484Ter)
GNPDA2 NM_138335.2 +?/. - c.*12252_*12255dup r.(=) p.(=)


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