Variant #0000000798 (NC_000023.10:g.56591248T>A, UBQLN2(NM_013444.3):c.942T>A)

Individual ID 00000798
Chromosome X
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.56591248T>A
Reference Kim HJ1, Kwon MJ2, Choi WJ3, Oh KW3, Oh SI3, Ki CS4, Kim SH5.(2014)
DB-ID UBQLN2_000001
Frequency -
Average frequency (gnomAD v.2.1.1) 5.0E-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     
UBQLN2 NM_013444.3 ./. 1 c.942T>A r.(?) p.(Asp314Glu) VariO:0136 DNA substitution; VariO:0316 transversion VariO:0021 amino acid substitution



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000798 ? ? UBQLN2 1 Y Yang