Variant #0000250503 (NC_000009.11:g.35738871A>G, NM_006368.4:c.*2148A>G (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.35738871A>G
DNA change (hg38) g.35738874A>G
Published as GBA2(NM_020944.3):c.1825T>C (p.Y609H)
ISCN -
DB-ID GBA2_000004
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RGP1 NM_001080496.2 +?/. - c.-10554A>G r.(?) p.(=)
TLN1 NM_006289.3 +?/. - c.-6833T>C r.(?) p.(=)
CREB3 NM_006368.4 +?/. - c.*2148A>G r.(=) p.(=)
GBA2 NM_020944.2 +?/. - c.1825T>C r.(?) p.(Tyr609His)


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