Variant #0000805473 (NC_000011.9:g.9168594T>C, NM_015213.3:c.2840A>G (DENND5A))

Chromosome 11
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.9168594T>C
DNA change (hg38) -
Published as DENND5A(NM_001348750.1):c.2552A>G (p.N851S), DENND5A(NM_015213.4):c.2840A>G (p.N947S)
ISCN -
DB-ID DENND5A_000023 See all 2 reported entries
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) 6.0E-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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2022-05-09 15:24:52 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DENND5A NM_015213.3 ?/. - c.2840A>G r.(?) p.(Asn947Ser)


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