Variant #0000526187 (NC_000005.9:g.82499423C>T, NM_022406.2:c.535C>T (XRCC4))

Chromosome 5
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.82499423C>T
DNA change (hg38) g.83203604C>T
Published as XRCC4(NM_022550.3):c.535C>T (p.R179W)
ISCN -
DB-ID TMEM167A_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) 7.0E-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 2019-07-18 18:22:55 +02:00 (CEST)
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     
XRCC4 NM_022406.2 ?/. - c.535C>T r.(?) p.(Arg179Trp)
TMEM167A NM_174909.4 ?/. - c.-126281G>A r.(?) p.(=)


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