Variant #0000681655 (NC_000020.10:g.57014075T>G, NM_004738.4:c.390T>G (VAPB))

Chromosome 20
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.57014075T>G
DNA change (hg38) -
Published as VAPB(NM_004738.4):c.390T>G (p.D130E, p.(Asp130Glu))
ISCN -
DB-ID VAPB_000007 See all 2 reported entries
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) 0.00125 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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
VAPB NM_001195677.1 -?/. - c.212-5058T>G r.(=) p.(=)
VAPB NM_004738.4 -?/. - c.390T>G r.(?) p.(Asp130Glu)


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