Unique variants in gene TAB2

Information The variants shown are described using the NM_015093.3 transcript reference sequence.

9 entries on 1 page. Showing entries 1 - 9.
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Effect     

Reported     

Exon     

AscendingDNA change (cDNA)     

Position     

RNA change     

Protein     

DNA change (genomic) (hg19)     

Reference     

DB-ID     

dbSNP ID     

Frequency     

Owner     
./. 1 - c.102+1902C>G - r.(=) p.(=) g.149693137C>G dbSNP TAB2_000001 rs9285520 0.75000 Admin
./. 1 - c.103-1394A>G - - - g.149697760A>G dbSNP TAB2_000002 rs9390676 0.86318 Admin
./. 1 - c.1603+1420C>G - r.(=) p.(=) g.149702074C>G dbSNP TAB2_000003 rs6934491 0.96959 Admin
./. 1 - c.1603+6634A>G - r.(=) p.(=) g.149707288A>G dbSNP TAB2_000004 rs9373589 0.38682 Admin
./. 1 - c.1603+6997C>T - - - g.149707651C>T dbSNP TAB2_000005 rs2341783 0.86486 Admin
./. 1 - c.1604-7892C>T - r.(=) p.(=) g.149710848C>T dbSNP TAB2_000006 rs237035 0.54223 Admin
./. 1 - c.1604-6757C>G - - - g.149711983C>G dbSNP TAB2_000007 rs9404034 0.84966 Admin
./. 1 - c.1939+1370A>G - - - g.149721690A>G dbSNP TAB2_000008 rs237025 0.47635 Admin
./. 1 - c.1939+4970A>G - - - g.149725290A>G dbSNP TAB2_000009 rs2789488 0.54899 Admin
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