Variant #0000000698 (NC_000020.10:g.57019259G>A, VAPB(NM_004738.4):c.700G>A)

Individual ID 00000698
Chromosome 20
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.57019259G>A
Reference van Blitterswijk M, van Es MA, Koppers M, van Rheenen W, Medic J, Schelhaas HJ, van der Kooi AJ, de Visser M, Veldink JH, van den Berg LH. (2012)
DB-ID VAPB_000003 See all 2 reported entries
Frequency -
Average frequency (gnomAD v.2.1.1) 6.0E-5 View details
Owner Y Yang
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Y Yang
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Variant/VariO/DNA     

Variant/VariO/protein     
VAPB NM_004738.4 +?/. 6 c.700G>A r.(?) p.(Val234Ile) VariO:0136 DNA substitution; VariO:0313 transition; VariO:0315 purine transition VariO:0021 amino acid substitution



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000698 ? ? C9orf72, VAPB 2 Y Yang