Variant #0000526572 (NC_000006.11:g.105606440G>A, NM_022361.4:c.781C>T (POPDC3))

Chromosome 6
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.105606440G>A
DNA change (hg38) g.105158565G>A
Published as POPDC3(NM_022361.4):c.781C>T (p.(Arg261Trp))
ISCN -
DB-ID POPDC3_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) 3.0E-5 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 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
POPDC3 NM_022361.4 -?/. - c.781C>T r.(?) p.(Arg261Trp)
BVES-AS1 NR_037157.1 -?/. - n.343-7979G>A r.(?) -


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