Variant #0000503486 (NC_000001.10:g.153907306_153907307insGC, NM_014856.2:c.2702_2703insGC (DENND4B))

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.153907306_153907307insGC
DNA change (hg38) g.153934830_153934831insGC
Published as DENND4B(NM_014856.3):c.2702_2703insGC (p.Q902Hfs*48)
ISCN -
DB-ID DENND4B_000008
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DENND4B NM_014856.2 -/. - c.2702_2703insGC r.(?) p.(Gln902HisfsTer48)


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