Variant #0000538130 (NC_000009.11:g.35740293C>G, NM_006368.4:c.*3570C>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.35740293C>G
DNA change (hg38) g.35740296C>G
Published as GBA2(NM_001330660.2):c.1196G>C (p.R399P), GBA2(NM_020944.2):c.1196G>C (p.R399P, p.(Arg399Pro))
ISCN -
DB-ID GBA2_000008 See all 3 reported entries
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) 0.0013 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RGP1 NM_001080496.2 -?/. - c.-9132C>G r.(?) p.(=)
TLN1 NM_006289.3 -?/. - c.-8255G>C r.(?) p.(=)
CREB3 NM_006368.4 -?/. - c.*3570C>G r.(=) p.(=)
GBA2 NM_020944.2 -?/. - c.1196G>C r.(?) p.(Arg399Pro)


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