Variant #0000337851 (NC_000009.11:g.35748806G>T, NM_006368.4:c.*12083G>T (CREB3))

Chromosome 9
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.35748806G>T
DNA change (hg38) g.35748809G>T
Published as -
ISCN -
DB-ID GBA2_000015
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MSMP NM_001044264.2 -/. - c.*4291C>A r.(=) p.(=)
RGP1 NM_001080496.2 -/. - c.-619G>T r.(?) p.(=)
CREB3 NM_006368.4 -/. - c.*12083G>T r.(=) p.(=)
GBA2 NM_020944.2 -/. - c.-105C>A r.(?) p.(=)


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