Variant #0000288397 (NC_000003.11:g.33114035C>T, NC_000003.11(NM_000404.2):c.245+1G>A (GLB1))

Chromosome 3
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.33114035C>T
DNA change (hg38) g.33072543C>T
Published as GLB1(NM_000404.3):c.245+1G>A
ISCN -
DB-ID GLB1_000041 See all 2 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 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 2020-06-12 15:22:54 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GLB1 NM_000404.2 +/. - c.245+1G>A r.spl? p.?
TMPPE NM_001039770.2 +/. - c.*20291G>A r.(=) p.(=)


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