Variant #0000005983 (NC_000009.11:g.?, VCP(NM_007126.3):c.?)

Individual ID 00005998
Chromosome 9
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.?
Reference Poksay KS et al. (2011)
DB-ID SIGMAR1_000001 See all 3 reported entries
Frequency -
Average frequency (gnomAD v.2.1.1) Genomic location of variant could not be determined
Owner XY Liu
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by XY Liu




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Variant/VariO/DNA     

Variant/VariO/protein     
VCP NM_007126.3 ./. 13 c.? r.(?) p.Lys524Ala - -



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000006017 ? ? VCP 3 XY Liu