Variant #0001014542 (NC_000009.11:g.35737387G>A, NM_006368.4:c.*664G>A (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.35737387G>A
DNA change (hg38) -
Published as GBA2(NM_020944.3):c.2563C>T (p.R855C)
ISCN -
DB-ID CREB3_000088
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) 3.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-10-29 21:08:56 +01:00 (CET)
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.-12038G>A r.(?) p.(=)
TLN1 NM_006289.3 ?/. - c.-5349C>T r.(?) p.(=)
CREB3 NM_006368.4 ?/. - c.*664G>A r.(=) p.(=)
GBA2 NM_020944.2 ?/. - c.2563C>T r.(?) p.(Arg855Cys)


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