All variants in the IL13RA2 gene

Information The variants shown are described using the NM_000640.2 transcript reference sequence.

6 entries on 1 page. Showing entries 1 - 6.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Owner     
?/. - c.331T>C r.(?) p.(Trp111Arg) - VUS g.114249053A>G g.115014490A>G - - IL13RA2_000001 found once, nonrecurrent change PubMed: Tarpey 2009 - - Germline - 1/208 cases - 0 - Lucy Raymond
-?/. - c.633T>C r.(?) p.(Tyr211=) - likely benign g.114245280A>G g.115010717A>G IL13RA2(NM_000640.2):c.633T>C (p.Y211=) - IL13RA2_000006 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Rotterdam
?/. - c.827T>C r.(?) p.(Ile276Thr) - VUS g.114244109A>G g.115009546A>G - - IL13RA2_000002 found once, nonrecurrent change PubMed: Tarpey 2009 - - Germline - 1/208 cases - 0 - Lucy Raymond
-?/. - c.845C>T r.(?) p.(Thr282Ile) - likely benign g.114244091G>A - IL13RA2(NM_000640.2):c.845C>T (p.T282I) - IL13RA2_000007 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Rotterdam
-?/. - c.905G>A r.(?) p.(Arg302Gln) - likely benign g.114242587C>T g.115008024C>T IL13RA2(NM_000640.2):c.905G>A (p.(Arg302Gln)) - IL13RA2_000003 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL_Leiden
-?/. - c.921A>C r.(?) p.(Val307=) - likely benign g.114242571T>G g.115008008T>G IL13RA2(NM_000640.2):c.921A>C (p.V307=) - IL13RA2_000005 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Rotterdam
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