Variant #0001053248 (NC_000009.11:g.35737226_35737241dup, NM_006368.4:c.*503_*518dup (CREB3))

Chromosome 9
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.35737226_35737241dup
DNA change (hg38) -
Published as GBA2(NM_020944.3):c.2710_2725dup (p.(Leu909Glnfs*49))
ISCN -
DB-ID CREB3_000094
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 2025-11-01 13:22:20 +01:00 (CET)
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.-12199_-12184dup r.(?) p.(=)
TLN1 NM_006289.3 ?/. - c.-5202_-5187dup r.(?) p.(=)
CREB3 NM_006368.4 ?/. - c.*503_*518dup r.(=) p.(=)
GBA2 NM_020944.2 ?/. - c.2710_2725dup r.(?) p.(Leu909Glnfs*49)


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