Variant #0000852276 (NC_000009.11:g.35738127G>T, NM_006368.4:c.*1404G>T (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.35738127G>T
DNA change (hg38) -
Published as GBA2(NM_001330660.1):c.2220C>A (p.S740R)
ISCN -
DB-ID GBA2_000016 See all 2 reported entries
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 15:40:45 +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     
RGP1 NM_001080496.2 ?/. - c.-11298G>T r.(?) p.(=)
TLN1 NM_006289.3 ?/. - c.-6089C>A r.(?) p.(=)
CREB3 NM_006368.4 ?/. - c.*1404G>T r.(=) p.(=)
GBA2 NM_020944.2 ?/. - c.2220C>A r.(?) p.(Ser740Arg)


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