Transcript #00004609

Transcript name transcript variant 156
Gene name DIAPH2 (diaphanous homolog 2 (Drosophila))
Chromosome X
Transcript - NCBI ID NM_006729.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_006720.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

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

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.-51C>T r.(=) p.(=)
?/? c.81C>T r.(=) p.(=)
?/? c.91C>T r.(?) p.(Arg31Trp)
?/? c.132+38_132+48del r.(=) p.(=)
?/? c.133-33del r.(=) p.(=)
?/? c.133-28_133-25del r.(=) p.(=)
?/? c.165+5G>C r.spl? p.?
?/? c.165+6G>C r.(=) p.(=)
?/? c.165+47_165+51del r.(=) p.(=)
?/? c.165+50A>T r.(=) p.(=)
?/? c.165+76T>C r.(=) p.(=)
?/? c.246C>T r.(=) p.(=)
?/? c.247G>A r.(?) p.(Ala83Thr)
?/? c.249G>A r.(=) p.(=)
?/? c.262C>T r.(?) p.(Pro88Ser)
?/? c.278T>C r.(?) p.(Leu93Ser)
?/? c.342+6T>C r.(=) p.(=)
?/? c.342+27A>G r.(=) p.(=)
?/? c.343-26C>T r.(=) p.(=)
?/? c.343-25C>T r.(=) p.(=)
?/? c.343-24C>T r.(=) p.(=)
?/? c.360C>T r.(=) p.(=)
?/? c.399C>T r.(=) p.(=)
?/? c.447+35359A>G r.(=) p.(=)
?/? c.587+25A>G r.(=) p.(=)
?/? c.587+2551G>C r.(=) p.(=)
?/? c.587+2605G>A r.(?) p.(Gly5Arg)
?/? c.587+2618A>G r.(?) p.(Tyr9Cys)
?/? c.587+2689G>A r.(?) p.(Ala33Thr)
?/? c.587+2727C>T r.(=) p.(=)
?/? c.587+2742T>C r.(=) p.(=)
?/? c.587+2751G>C r.(?) p.(Gln53His)
?/? c.587+2953G>T r.(?) p.(Val121Phe)
?/? c.587+2956G>A r.(?) p.(Gly122Arg)
?/? c.587+2987A>G r.(?) p.(Lys132Arg)
?/? c.587+2999G>A r.(?) p.(Gly136Glu)
?/? c.587+3012T>A r.(=) p.(=)
?/? c.587+3029A>G r.(?) p.(His146Arg)
?/? c.587+3054C>T r.(=) p.(=)
?/? c.587+3058G>A r.(?) p.(Val156Met)
?/? c.587+3064A>G r.(?) p.(Ile158Val)
?/? c.587+3160G>T r.(?) p.(Ala190Ser)
?/? c.587+3184C>T r.(?) p.(Arg198Cys)
?/? c.587+3241G>A r.(?) p.(Gly217Arg)
?/? c.587+3348G>T r.(=) p.(=)
?/? c.587+3357G>A r.(=) p.(=)
?/? c.587+3399A>G r.(=) p.(=)
?/? c.588-39T>C r.(=) p.(=)
?/? c.588C>T r.(=) p.(=)
?/? c.657A>G r.(=) p.(=)
?/? c.677A>T r.(?) p.(Asp226Val)
?/? c.733-15_733-14insTC r.(=) p.(=)
?/? c.790A>G r.(?) p.(Ile264Val)
?/? c.869+47T>G r.(=) p.(=)
?/? c.869+49A>G r.(=) p.(=)
?/? c.870-8C>G r.(=) p.(=)
?/? c.975A>G r.(=) p.(=)
?/? c.978+28C>G r.(=) p.(=)
?/? c.979-26A>T r.(=) p.(=)
?/? c.1032T>C r.(=) p.(=)
?/? c.1063C>T r.(?) p.(Arg355Cys)
?/? c.1196G>A r.(?) p.(Arg399Gln)
?/? c.1208+11A>G r.(=) p.(=)
?/? c.1208+37A>C r.(=) p.(=)
?/? c.1209-50T>C r.(=) p.(=)
?/? c.1231C>T r.(?) p.(Leu411Phe)
?/? c.1259C>A r.(?) p.(Ala420Asp)
?/? c.1275C>G r.(?) p.(Phe425Leu)
?/? c.1295T>G r.(?) p.(Phe432Cys)
?/? c.1312G>T r.(?) p.(Asp438Tyr)
?/? c.1325+25A>G r.(=) p.(=)
?/? c.1325+26T>G r.(=) p.(=)
?/? c.1325+42C>T r.(=) p.(=)
?/? c.1329A>T r.(=) p.(=)
?/? c.1334A>G r.(?) p.(Tyr445Cys)
?/? c.1444+40G>A r.(=) p.(=)
?/? c.1445-26G>A r.(=) p.(=)
?/? c.1464G>A r.(=) p.(=)
?/? c.1477A>G r.(?) p.(Ser493Gly)
?/? c.1509+28C>T r.(=) p.(=)
?/? c.1509+29G>A r.(=) p.(=)
?/? c.1510-48G>A r.(=) p.(=)
?/? c.1510-32T>C r.(=) p.(=)
?/? c.1510-4G>A r.spl? p.?
?/? c.1512C>T r.(=) p.(=)
?/? c.1513G>C r.(?) p.(Asp505His)
?/? c.1547C>T r.(?) p.(Ala516Val)
?/? c.1586A>C r.(?) p.(Glu529Ala)
?/? c.1600C>G r.(?) p.(Gln534Glu)
?/? c.1621G>A r.(?) p.(Val541Ile)
?/? c.1701C>T r.(=) p.(=)
?/? c.1702G>A r.(?) p.(Ala568Thr)
?/? c.1703C>T r.(?) p.(Ala568Val)
?/? c.1716C>T r.(=) p.(=)
?/? c.1773A>G r.(=) p.(=)
?/? c.1792C>G r.(?) p.(Leu598Val)
?/? c.1794T>C r.(=) p.(=)
?/? c.1822C>A r.(?) p.(Pro608Thr)
?/? c.1834G>A r.(?) p.(Val612Ile)
?/? c.1847C>T r.(?) p.(Pro616Leu)
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