Variant #0000693762 (NC_000023.10:g.79938022G>A, BRWD3(NM_153252.4):c.4339C>T)

Chromosome X
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.79938022G>A
DNA change (hg38) -
Published as BRWD3(NM_153252.4):c.4339C>T (p.R1447W), BRWD3(NM_153252.5):c.4339C>T (p.R1447W)
ISCN -
DB-ID BRWD3_000055 See all 3 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) 2.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BRWD3 NM_153252.4 ?/. - c.4339C>T r.(?) p.(Arg1447Trp)