Variant #0000723439 (NC_000011.9:g.36615075G>A, NM_000536.2:c.644C>T (RAG2))

Chromosome 11
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.36615075G>A
DNA change (hg38) -
Published as RAG2(NM_000536.4):c.644C>T (p.T215I), RAG2(NM_001243786.1):c.644C>T (p.T215I)
ISCN -
DB-ID RAG2_000021 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) 0.00332 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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RAG2 NM_000536.2 -/. - c.644C>T r.(?) p.(Thr215Ile)
C11orf74 NM_138787.2 -/. - c.-1091G>A r.(?) p.(=)


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