Variant #0000804117 (NC_000009.11:g.35703768C>T, NM_006368.4:c.-29002C>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.35703768C>T
DNA change (hg38) -
Published as TLN1(NM_006289.4):c.6357+4G>A
ISCN -
DB-ID CREB3_000035
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TLN1 NM_006289.3 -?/. - c.6357+4G>A r.spl? p.?
CREB3 NM_006368.4 -?/. - c.-29002C>T r.(?) p.(=)


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