All variants in the TNFAIP3 gene

Information The variants shown are described using the NM_006290.3 transcript reference sequence.

2 entries on 1 page. Showing entries 1 - 2.
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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.2231G>A r.(?) p.(Gly744Asp) - likely benign g.138202314G>A g.137881177G>A TNFAIP3(NM_001270508.1):c.2231G>A (p.G744D), TNFAIP3(NM_001270508.2):c.2231G>A (p.G744D) - TNFAIP3_000007 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL_Utrecht
-?/. - c.2231G>A r.(?) p.(Gly744Asp) - likely benign g.138202314G>A g.137881177G>A TNFAIP3(NM_001270508.1):c.2231G>A (p.G744D), TNFAIP3(NM_001270508.2):c.2231G>A (p.G744D) - TNFAIP3_000007 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Rotterdam
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