Variant #0000723440 (NC_000011.9:g.36615367del, NM_000536.2:c.356del (RAG2))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.36615367del
DNA change (hg38) -
Published as RAG2(NM_001243786.1):c.356delA (p.K119Rfs*12)
ISCN -
DB-ID RAG2_000022
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RAG2 NM_000536.2 +?/. - c.356del r.(?) p.(Lys119Argfs*12)
C11orf74 NM_138787.2 +?/. - c.-799del r.(?) p.(=)


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