All variants in the GLB1 gene

Information The variants shown are described using the NM_000404.2 transcript reference sequence.

4 entries on 1 page. Showing entries 1 - 4.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Owner     
-/. - c.1594A>G r.(?) p.(Ser532Gly) - benign g.33055688T>C g.33014196T>C GLB1(NM_000404.2):c.1594A>G (p.(Ser532Gly)), GLB1(NM_000404.3):c.1594A>G (p.S532G) - GLB1_000039 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL_Groningen
-/. - c.1594A>G r.(?) p.(Ser532Gly) - benign g.33055688T>C g.33014196T>C GLB1(NM_000404.2):c.1594A>G (p.(Ser532Gly)), GLB1(NM_000404.3):c.1594A>G (p.S532G) - GLB1_000039 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL_Rotterdam
-?/. - c.1594A>G r.(?) p.(Ser532Gly) - likely benign g.33055688T>C g.33014196T>C GLB1(NM_000404.2):c.1594A>G (p.(Ser532Gly)), GLB1(NM_000404.3):c.1594A>G (p.S532G) - GLB1_000039 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Leiden
-/. - c.1594A>G r.(?) p.(Ser532Gly) - benign g.33055688T>C g.33014196T>C GLB1(NM_000404.2):c.1594A>G (p.(Ser532Gly)), GLB1(NM_000404.3):c.1594A>G (p.S532G) - GLB1_000039 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Nijmegen
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