All variants in the TNFAIP3 gene

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

3 entries on 1 page. Showing entries 1 - 3.
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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.380T>G r.(?) p.(Phe127Cys) - VUS g.138196066T>G g.137874929T>G - - TNFAIP3_000021 no interpretation available; 175 heterozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs2230926 Germline - 175/2795 individuals - 0 - Mohammed Faruq
?/. - c.380T>G r.(?) p.(Phe127Cys) - VUS g.138196066T>G g.137874929T>G - - TNFAIP3_000021 no interpretation available; 2 homozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs2230926 Germline - 2/2795 individuals - 0 - Mohammed Faruq
-/. - c.380T>G r.(?) p.(Phe127Cys) - benign g.138196066T>G - TNFAIP3(NM_006290.3):c.380T>G (p.F127C) - TNFAIP3_000021 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Groningen
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