Variant #0000886922 (NC_000005.9:g.82499501C>T, NM_022406.2:c.613C>T (XRCC4))

Chromosome 5
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.82499501C>T
DNA change (hg38) -
Published as XRCC4(NM_022406.5):c.613C>T (p.R205*)
ISCN -
DB-ID TMEM167A_000004
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +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.613C>T r.(?) p.(Arg205*)
TMEM167A NM_174909.4 +/. - c.-126359G>A r.(?) p.(=)


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