Variant #0000323404 (NC_000013.10:g.50102794C>A, NM_018191.3:c.*5464G>T (RCBTB1))

Chromosome 13
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.50102794C>A
DNA change (hg38) g.49528658C>A
Published as PHF11(NM_001040443.1):c.989C>A (p.(Ser330Tyr))
ISCN -
DB-ID PHF11_000002
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) 0.00261 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     
PHF11 NM_001040443.1 ?/. - c.989C>A r.(?) p.(Ser330Tyr)
RCBTB1 NM_018191.3 ?/. - c.*5464G>T r.(=) p.(=)
SETDB2 NM_031915.2 ?/. - c.*36809C>A r.(=) p.(=)


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