Variant #0000975753 (NC_000003.11:g.33114153T>C, NM_000404.2:c.128A>G (GLB1))

Chromosome 3
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.33114153T>C
DNA change (hg38) -
Published as GLB1(NM_000404.4):c.128A>G (p.(Lys43Arg))
ISCN -
DB-ID GLB1_000121
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GLB1 NM_000404.2 ?/. - c.128A>G r.(?) p.(Lys43Arg)
TMPPE NM_001039770.2 ?/. - c.*20173A>G r.(=) p.(=)


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