Variant #0000301348 (NC_000011.9:g.36614561G>T, NM_000536.2:c.1158C>A (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.36614561G>T
DNA change (hg38) g.36593011G>T
Published as RAG2(NM_001243786.1):c.1158C>A (p.F386L), RAG2(NM_001243786.2):c.1158C>A (p.F386L)
ISCN -
DB-ID RAG2_000003 See all 3 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) 0.00965 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 2018-01-15 20:58:59 +01:00 (CET)
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.1158C>A r.(?) p.(Phe386Leu)
C11orf74 NM_138787.2 -?/. - c.-1605G>T r.(?) p.(=)


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