Variant #0000678672 (NC_000009.11:g.35744673A>C, NM_006368.4:c.*7950A>C (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.35744673A>C
DNA change (hg38) -
Published as GBA2(NM_020944.2):c.390T>G (p.(His130Gln))
ISCN -
DB-ID CREB3_000026
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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MSMP NM_001044264.2 -?/. - c.*8424T>G r.(=) p.(=)
RGP1 NM_001080496.2 -?/. - c.-4752A>C r.(?) p.(=)
CREB3 NM_006368.4 -?/. - c.*7950A>C r.(=) p.(=)
GBA2 NM_020944.2 -?/. - c.390T>G r.(?) p.(His130Gln)


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