Variant #0000622628 (NC_000011.9:g.36614624A>G, NM_000536.2:c.1095T>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.36614624A>G
DNA change (hg38) g.36593074A>G
Published as RAG2(NM_001243786.1):c.1095T>C (p.S365=)
ISCN -
DB-ID RAG2_000004 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) 0.00163 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-06 12:43:26 +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.1095T>C r.(?) p.(=)
C11orf74 NM_138787.2 -?/. - c.-1542A>G r.(?) p.(=)


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