Transcript #00015931 (NM_001242359.1, RHOBTB1 gene)

Transcript name transcript variant 4
Gene name RHOBTB1 (Rho-related BTB domain containing 1)
Chromosome 10
Transcript - NCBI ID NM_001242359.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001229288.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

112 entries on 2 pages. Showing entries 1 - 100.
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Affects function     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.-5C>T r.(=) p.(=)
?/? c.6C>T r.(=) p.(=)
?/? c.18C>T r.(=) p.(=)
?/? c.21C>T r.(=) p.(=)
?/? c.33C>T r.(=) p.(=)
?/? c.91A>G r.(?) p.(Ile31Val)
?/? c.165G>A r.(=) p.(=)
?/? c.178C>T r.(?) p.(Arg60Cys)
?/? c.192+17G>A r.(=) p.(=)
?/? c.192+37A>G r.(=) p.(=)
?/? c.193-31C>T r.(=) p.(=)
?/? c.193-30G>A r.(=) p.(=)
?/? c.296+21C>T r.(=) p.(=)
?/? c.296+22G>A r.(=) p.(=)
?/? c.296+25G>A r.(=) p.(=)
?/? c.296+41A>G r.(=) p.(=)
?/? c.296+42T>C r.(=) p.(=)
?/? c.297-33G>A r.(=) p.(=)
?/? c.297-19T>G r.(=) p.(=)
?/? c.349C>G r.(?) p.(His117Asp)
?/? c.375A>G r.(=) p.(=)
?/? c.403G>A r.(?) p.(Val135Ile)
?/? c.417G>T r.(=) p.(=)
?/? c.433C>T r.(?) p.(Arg145Cys)
?/? c.441C>T r.(=) p.(=)
?/? c.442G>A r.(?) p.(Asp148Asn)
?/? c.451G>T r.(?) p.(Ala151Ser)
?/? c.474G>A r.(=) p.(=)
?/? c.482+27T>A r.(=) p.(=)
?/? c.482+35C>T r.(=) p.(=)
?/? c.483-45_483-44insT r.(=) p.(=)
?/? c.483-20T>G r.(=) p.(=)
?/? c.540A>G r.(=) p.(=)
?/? c.545G>T r.(?) p.(Gly182Val)
?/? c.570G>A r.(=) p.(=)
?/? c.614G>A r.(?) p.(Arg205Gln)
?/? c.685C>T r.(?) p.(Leu229Phe)
?/? c.691G>A r.(?) p.(Ala231Thr)
?/? c.712G>T r.(?) p.(Ala238Ser)
?/? c.734T>C r.(?) p.(Ile245Thr)
?/? c.738A>G r.(=) p.(=)
?/? c.756G>A r.(=) p.(=)
?/? c.769G>C r.(?) p.(Ala257Pro)
?/? c.773G>A r.(?) p.(Cys258Tyr)
?/? c.856G>A r.(?) p.(Ala286Thr)
?/? c.934G>A r.(?) p.(Glu312Lys)
?/? c.968G>A r.(?) p.(Arg323Gln)
?/? c.969G>C r.(=) p.(=)
?/? c.981C>G r.(=) p.(=)
?/? c.1010C>T r.(?) p.(Pro337Leu)
?/? c.1034A>G r.(?) p.(Gln345Arg)
?/? c.1055G>A r.(?) p.(Ser352Asn)
?/? c.1059G>A r.(=) p.(=)
?/? c.1165C>T r.(?) p.(Pro389Ser)
?/? c.1234C>T r.(?) p.(Arg412Trp)
?/? c.1258A>G r.(?) p.(Thr420Ala)
?/? c.1329C>T r.(=) p.(=)
?/? c.1392G>A r.(=) p.(=)
?/? c.1418A>G r.(?) p.(Asn473Ser)
?/? c.1421G>C r.(?) p.(Arg474Pro)
?/? c.1455G>C r.(=) p.(=)
?/? c.1456+12G>A r.(=) p.(=)
?/? c.1457-43A>C r.(=) p.(=)
?/? c.1457-16C>T r.(=) p.(=)
?/? c.1458C>T r.(=) p.(=)
?/? c.1477G>A r.(?) p.(Asp493Asn)
?/? c.1478A>G r.(?) p.(Asp493Gly)
?/? c.1543G>A r.(?) p.(Gly515Arg)
?/? c.1572T>C r.(=) p.(=)
?/? c.1575+28T>A r.(=) p.(=)
?/? c.1575+47G>T r.(=) p.(=)
?/? c.1668G>A r.(=) p.(=)
?/? c.1717G>T r.(?) p.(Ala573Ser)
?/? c.1726+27A>G r.(=) p.(=)
?/? c.1727-39C>T r.(=) p.(=)
?/? c.1727-16C>G r.(=) p.(=)
?/? c.1727-15C>A r.(=) p.(=)
?/? c.1727-7del r.(=) p.(=)
?/? c.1727-6C>T r.(=) p.(=)
?/? c.1738G>A r.(?) p.(Val580Ile)
?/? c.1758C>T r.(=) p.(=)
?/? c.1770C>T r.(=) p.(=)
?/? c.1782C>T r.(=) p.(=)
?/? c.1798T>C r.(?) p.(Tyr600His)
?/? c.1807T>C r.(=) p.(=)
?/? c.1816-44C>T r.(=) p.(=)
?/? c.1816-32G>A r.(=) p.(=)
?/? c.1816-28T>C r.(=) p.(=)
?/? c.1816-14T>C r.(=) p.(=)
?/? c.1816-6C>T r.(=) p.(=)
?/? c.1823A>G r.(?) p.(Asn608Ser)
?/? c.1840G>T r.(?) p.(Ala614Ser)
?/? c.1841C>T r.(?) p.(Ala614Val)
?/? c.1849T>C r.(=) p.(=)
?/? c.1856A>G r.(?) p.(His619Arg)
?/? c.1886C>G r.(?) p.(Ser629Cys)
?/? c.1921+18C>T r.(=) p.(=)
?/? c.1921+40A>T r.(=) p.(=)
?/? c.1922-50A>C r.(=) p.(=)
?/? c.1922-34G>A r.(=) p.(=)
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