Variant #0000006633 (NC_000002.11:g.202609041G>A, ALS2(NM_020919.3):c.2110C>T)

Individual ID 00006638
Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.202609041G>A
Reference Yousef Daneshmandpour, et al. (2023)
DB-ID ALS2_000026
Frequency -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner XY Liu
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by XY Liu
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Variant/VariO/DNA     

Variant/VariO/protein     
ALS2 NM_020919.3 ?/. 10 c.2110C>T r.(2110c>u) p.(Arg704*) - -



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000006662 ? ? ALS2 1 XY Liu