Variant #0000321006 (NC_000001.10:g.153920969G>T, NM_014856.2:c.-2216C>A (DENND4B))

Chromosome 1
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.153920969G>T
DNA change (hg38) g.153948493G>T
Published as CRTC2(NM_181715.2):c.1826C>A (p.(Ser609Tyr))
ISCN -
DB-ID CRTC2_000001
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 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DENND4B NM_014856.2 ?/. - c.-2216C>A r.(?) p.(=)
CRTC2 NM_181715.2 ?/. - c.1826C>A r.(?) p.(Ser609Tyr)


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