Variant #0000401100 (NC_000023.10:g.103267974G>A, H2BFWT(NM_001002916.3):c.259C>T)

Individual ID 00173642
Chromosome X
Allele Parent #1
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.103267974G>A
DNA change (hg38) g.104013402G>A
Published as R87W
ISCN -
DB-ID H2BFWT_000008
Variant remarks recurrent, found 6 times
Reference PubMed: Tarpey 2009
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency 6/208 cases
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.0166 View details
Owner Lucy Raymond
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2009-05-08 12:40:34 +02:00 (CEST)
Date last edited 2009-05-19 12:34:20 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
H2BFWT NM_001002916.3 ?/. 1 c.259C>T r.(?) p.(Arg87Trp)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000174525 DNA SEQ - - ARMCX6 1 Lucy Raymond