Variant #0000262379 (NC_000002.11:g.202625615C>T, NM_020919.3:c.1102G>A (ALS2))

Chromosome 2
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.202625615C>T
DNA change (hg38) g.201760892C>T
Published as ALS2(NM_020919.3):c.1102G>A (p.V368M), ALS2(NM_020919.4):c.1102G>A (p.V368M)
ISCN -
DB-ID ALS2_000036 See all 6 reported entries
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) 0.91295 View details
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 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ALS2 NM_020919.3 -/. - c.1102G>A r.(?) p.(Val368Met)


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