Variant #0000861645 (NC_000009.11:g.35748376C>T, NM_006368.4:c.*11653C>T (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.35748376C>T
DNA change (hg38) -
Published as GBA2(NM_020944.2):c.326G>A (p.S109N)
ISCN -
DB-ID CREB3_000052
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) 0.00048 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 2022-05-09 15:51:19 +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.*4721G>A r.(=) p.(=)
RGP1 NM_001080496.2 -?/. - c.-1049C>T r.(?) p.(=)
CREB3 NM_006368.4 -?/. - c.*11653C>T r.(=) p.(=)
GBA2 NM_020944.2 -?/. - c.326G>A r.(?) p.(Ser109Asn)


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