Variant #0000172019 (NC_000012.11:g.108958089G>A, ISCU(NM_014301.3):c.74G>A)

Chromosome 12
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Effect unknown
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.108958089G>A
DNA change (hg38) g.108564313G>A
Published as 149G>A (Gly50Glu)
ISCN -
DB-ID ISCU_000002
Variant remarks -
Reference {PMID9:Kollberg 2009:1956769}, OMIM:var0002
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2010-11-14 16:47:50 +01:00 (CET)
Date last edited 2017-06-28 22:52:41 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ISCU NM_014301.3 +/? 3 c.74G>A r.(?) p.(Gly25Glu)