Variant #0000288393 (NC_000003.11:g.33058254G>A, GLB1(NM_000404.2):c.1426C>T)

Chromosome 3
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.33058254G>A
DNA change (hg38) g.33016762G>A
Published as GLB1(NM_001317040.1):c.1570C>T (p.L524=)
ISCN -
DB-ID GLB1_000049
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00056 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GLB1 NM_000404.2 -?/. - c.1426C>T r.(?) p.(Leu476=)
TMPPE NM_001039770.2 -?/. - c.*76072C>T r.(=) p.(=)