Variant #0000920860 (NC_000001.10:g.100368302C>T, NM_000642.2:c.3652C>T (AGL))

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.100368302C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID AGL_000094
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs771853367
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2023-03-10 11:19:01 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AGL NM_000642.2 +/. - c.3652C>T r.(?) p.(Arg1218Ter)


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