Variant #0000288395 (NC_000003.11:g.33055688T>C, GLB1(NM_000404.2):c.1594A>G)

Chromosome 3
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.33055688T>C
DNA change (hg38) g.33014196T>C
Published as GLB1(NM_000404.2):c.1594A>G (p.(Ser532Gly)), GLB1(NM_000404.3):c.1594A>G (p.S532G)
ISCN -
DB-ID GLB1_000039 See all 4 reported entries
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) 0.04691 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.1594A>G r.(?) p.(Ser532Gly)
TMPPE NM_001039770.2 -/. - c.*78638A>G r.(=) p.(=)