Variant #0000804122 (NC_000009.11:g.35748436C>G, NM_006368.4:c.*11713C>G (CREB3))

Chromosome 9
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.35748436C>G
DNA change (hg38) -
Published as GBA2(NM_020944.2):c.266G>C (p.C89S)
ISCN -
DB-ID CREB3_000040
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) 5.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +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     
MSMP NM_001044264.2 -?/. - c.*4661G>C r.(=) p.(=)
RGP1 NM_001080496.2 -?/. - c.-989C>G r.(?) p.(=)
CREB3 NM_006368.4 -?/. - c.*11713C>G r.(=) p.(=)
GBA2 NM_020944.2 -?/. - c.266G>C r.(?) p.(Cys89Ser)


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