Variant #0000543878 (NC_000011.9:g.36614528A>G, NM_000536.2:c.1191T>C (RAG2))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.36614528A>G
DNA change (hg38) g.36592978A>G
Published as RAG2(NM_001243786.1):c.1191T>C (p.D397=)
ISCN -
DB-ID RAG2_000011
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +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     
RAG2 NM_000536.2 -?/. - c.1191T>C r.(?) p.(=)
C11orf74 NM_138787.2 -?/. - c.-1638A>G r.(?) p.(=)


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