Variant #0000976869 (NC_000005.9:g.82491754C>T, NM_022406.2:c.481C>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.82491754C>T
DNA change (hg38) -
Published as XRCC4(NM_003401.5):c.481C>T (p.(Arg161Ter))
ISCN -
DB-ID XRCC4_000003 See all 2 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) 1.0E-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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
XRCC4 NM_022406.2 ?/. - c.481C>T r.(?) p.(Arg161*)
TMEM167A NM_174909.4 ?/. - c.-118612G>A r.(?) p.(=)


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