Variant #0000538123 (NC_000009.11:g.35735134G>A, NM_006368.4:c.464G>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.35735134G>A
DNA change (hg38) g.35735137G>A
Published as CREB3(NM_006368.4):c.464G>A (p.(Arg155Gln))
ISCN -
DB-ID CREB3_000005
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) 0.00105 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RGP1 NM_001080496.2 ?/. - c.-14291G>A r.(?) p.(=)
TLN1 NM_006289.3 ?/. - c.-3096C>T r.(?) p.(=)
CREB3 NM_006368.4 ?/. - c.464G>A r.(?) p.(Arg155Gln)
GBA2 NM_020944.2 ?/. - c.*2032C>T r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.