Variant #0000262072 (NC_000001.10:g.100366213G>A, NM_000642.2:c.3384G>A (AGL))

Chromosome 1
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.100366213G>A
DNA change (hg38) g.99900657G>A
Published as AGL(NM_000028.2):c.3384G>A (p.A1128=, p.(Ala1128=)), AGL(NM_000642.3):c.3384G>A (p.A1128=)
ISCN -
DB-ID AGL_000039 See all 3 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) 0.00091 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 2024-04-19 20:20:39 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AGL NM_000642.2 -/. - c.3384G>A r.(?) p.(Ala1128=)


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