Variant #0000538129 (NC_000009.11:g.35740047C>T, NM_006368.4:c.*3324C>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.35740047C>T
DNA change (hg38) g.35740050C>T
Published as GBA2(NM_001330660.1):c.1357G>A (p.A453T)
ISCN -
DB-ID CREB3_000011
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) 5.0E-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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RGP1 NM_001080496.2 -?/. - c.-9378C>T r.(?) p.(=)
TLN1 NM_006289.3 -?/. - c.-8009G>A r.(?) p.(=)
CREB3 NM_006368.4 -?/. - c.*3324C>T r.(=) p.(=)
GBA2 NM_020944.2 -?/. - c.1357G>A r.(?) p.(Ala453Thr)


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