Variant #0001037516 (NC_000009.11:g.35737342G>A, NM_006368.4:c.*619G>A (CREB3))

Chromosome 9
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.35737342G>A
DNA change (hg38) -
Published as GBA2(NM_020944.3):c.2608C>T (p.(Arg870Ter))
ISCN -
DB-ID CREB3_000093
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 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RGP1 NM_001080496.2 +?/. - c.-12083G>A r.(?) p.(=)
TLN1 NM_006289.3 +?/. - c.-5304C>T r.(?) p.(=)
CREB3 NM_006368.4 +?/. - c.*619G>A r.(=) p.(=)
GBA2 NM_020944.2 +?/. - c.2608C>T r.(?) p.(Arg870*)


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