Variant #0000288251 (NC_000009.11:g.35744638T>C, NM_006368.4:c.*7915T>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.35744638T>C
DNA change (hg38) g.35744641T>C
Published as GBA2(NM_020944.2):c.425A>G (p.N142S)
ISCN -
DB-ID GBA2_000010
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) 1.0E-5 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MSMP NM_001044264.2 -?/. - c.*8459A>G r.(=) p.(=)
RGP1 NM_001080496.2 -?/. - c.-4787T>C r.(?) p.(=)
CREB3 NM_006368.4 -?/. - c.*7915T>C r.(=) p.(=)
GBA2 NM_020944.2 -?/. - c.425A>G r.(?) p.(Asn142Ser)


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