Variant #0000319500 (NC_000020.10:g.57016045_57016047del, NM_004738.4:c.479_481del (VAPB))

Chromosome 20
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.57016045_57016047del
DNA change (hg38) g.58440989_58440991del
Published as VAPB(NM_004738.4):c.479_481delCTT (p.S160del), VAPB(NM_004738.5):c.479_481delCTT (p.S160del)
ISCN -
DB-ID VAPB_000002
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 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
VAPB NM_001195677.1 -/. - c.212-3088_212-3086del r.(=) p.(=)
VAPB NM_004738.4 -/. - c.479_481del r.(?) p.(Ser160del)


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