All transcript variants in gene ARHGAP36

Information The variants shown are described using the NM_144967.3 transcript reference sequence.

72 entries on 1 page. Showing entries 1 - 72.
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Effect     

AscendingDNA change (cDNA)     

RNA change     

Protein     

DNA change (genomic) (hg19)     

Reference     

DB-ID     

Frequency     

Freq. EA     

Freq. AA     
?/? c.-10C>T r.(=) p.(=) g.130215630C>T Copied from the Exome Variant Server ARHGAP36_000001 4/10563 3/6728 1/3835
?/? c.15T>A r.(=) p.(=) g.130215654T>A Copied from the Exome Variant Server ARHGAP36_000002 1/10563 1/6728 0/3835
?/? c.82T>C r.(?) p.(Phe28Leu) g.130215721T>C Copied from the Exome Variant Server ARHGAP36_000003 1/10563 1/6728 0/3835
?/? c.95T>C r.(?) p.(Val32Ala) g.130215734T>C Copied from the Exome Variant Server ARHGAP36_000004 1/10563 0/6728 1/3835
?/? c.129C>G r.(=) p.(=) g.130215768C>G Copied from the Exome Variant Server ARHGAP36_000005 12/10563 11/6728 1/3835
?/? c.134G>T r.(?) p.(Arg45Leu) g.130215773G>T Copied from the Exome Variant Server ARHGAP36_000006 1/10563 1/6728 0/3835
?/? c.253+12C>T r.(=) p.(=) g.130215904C>T Copied from the Exome Variant Server ARHGAP36_000007 1/10563 0/6728 1/3835
?/? c.253+49C>T r.(=) p.(=) g.130215941C>T Copied from the Exome Variant Server ARHGAP36_000008 2/10550 2/6717 0/3833
?/? c.254-47T>C r.(=) p.(=) g.130217092T>C Copied from the Exome Variant Server ARHGAP36_000009 1/10561 1/6728 0/3833
?/? c.254-41C>T r.(=) p.(=) g.130217098C>T Copied from the Exome Variant Server ARHGAP36_000010 9/10560 8/6727 1/3833
?/? c.254-31A>T r.(=) p.(=) g.130217108A>T Copied from the Exome Variant Server ARHGAP36_000011 2/10563 0/6728 2/3835
?/? c.254-24_254-23insT r.(=) p.(=) g.130217115_130217116insT Copied from the Exome Variant Server ARHGAP36_000012 19/10205 18/6484 1/3721
?/? c.283G>A r.(?) p.(Asp95Asn) g.130217168G>A Copied from the Exome Variant Server ARHGAP36_000013 2/10563 2/6728 0/3835
?/? c.288G>A r.(=) p.(=) g.130217173G>A Copied from the Exome Variant Server ARHGAP36_000014 37/10563 0/6728 37/3835
?/? c.319+42G>C r.(=) p.(=) g.130217246G>C Copied from the Exome Variant Server ARHGAP36_000015 1/10563 1/6728 0/3835
?/? c.320-25C>A r.(=) p.(=) g.130217683C>A Copied from the Exome Variant Server ARHGAP36_000016 1/10563 1/6728 0/3835
?/? c.377C>T r.(?) p.(Thr126Ile) g.130217765C>T Copied from the Exome Variant Server ARHGAP36_000017 1/10563 0/6728 1/3835
?/? c.378C>T r.(=) p.(=) g.130217766C>T Copied from the Exome Variant Server ARHGAP36_000018 112/10563 109/6728 3/3835
?/? c.403G>C r.(?) p.(Ala135Pro) g.130217791G>C Copied from the Exome Variant Server ARHGAP36_000019 1/10563 1/6728 0/3835
?/? c.446G>A r.(?) p.(Arg149His) g.130217834G>A Copied from the Exome Variant Server ARHGAP36_000020 1/10563 1/6728 0/3835
?/? c.448C>G r.(?) p.(Arg150Gly) g.130217836C>G Copied from the Exome Variant Server ARHGAP36_000021 1/10563 1/6728 0/3835
?/? c.488G>A r.(?) p.(Arg163Gln) g.130217876G>A Copied from the Exome Variant Server ARHGAP36_000022 2/10563 0/6728 2/3835
?/? c.516G>A r.(=) p.(=) g.130217904G>A Copied from the Exome Variant Server ARHGAP36_000023 3/10563 2/6728 1/3835
?/? c.555+13C>A r.(=) p.(=) g.130217956C>A Copied from the Exome Variant Server ARHGAP36_000024 6/10538 6/6707 0/3831
?/? c.555+43G>T r.(=) p.(=) g.130217986G>T Copied from the Exome Variant Server ARHGAP36_000025 5/10434 4/6650 1/3784
?/? c.556-47T>C r.(=) p.(=) g.130218142T>C Copied from the Exome Variant Server ARHGAP36_000026 4/10561 0/6726 4/3835
?/? c.556-46G>A r.(=) p.(=) g.130218143G>A Copied from the Exome Variant Server ARHGAP36_000027 1/10561 1/6726 0/3835
?/? c.562G>A r.(?) p.(Val188Met) g.130218195G>A Copied from the Exome Variant Server ARHGAP36_000028 1/10562 0/6727 1/3835
?/? c.721G>A r.(?) p.(Ala241Thr) g.130218354G>A Copied from the Exome Variant Server ARHGAP36_000029 1/10563 1/6728 0/3835
?/? c.748+15A>G r.(=) p.(=) g.130218396A>G Copied from the Exome Variant Server ARHGAP36_000030 1/10562 0/6727 1/3835
?/? c.749-20C>T r.(=) p.(=) g.130218580C>T Copied from the Exome Variant Server ARHGAP36_000031 1/10563 1/6728 0/3835
?/? c.757G>A r.(?) p.(Ala253Thr) g.130218608G>A Copied from the Exome Variant Server ARHGAP36_000032 1/10563 1/6728 0/3835
?/? c.763G>C r.(?) p.(Gly255Arg) g.130218614G>C Copied from the Exome Variant Server ARHGAP36_000033 1/10563 0/6728 1/3835
?/? c.805-48G>C r.(=) p.(=) g.130218840G>C Copied from the Exome Variant Server ARHGAP36_000034 3/10563 1/6728 2/3835
?/? c.805-22C>T r.(=) p.(=) g.130218866C>T Copied from the Exome Variant Server ARHGAP36_000035 1/10563 0/6728 1/3835
?/? c.884A>G r.(?) p.(Lys295Arg) g.130218967A>G Copied from the Exome Variant Server ARHGAP36_000036 2/10563 2/6728 0/3835
?/? c.885G>A r.(=) p.(=) g.130218968G>A Copied from the Exome Variant Server ARHGAP36_000037 30/10563 0/6728 30/3835
?/? c.924T>C r.(=) p.(=) g.130219007T>C Copied from the Exome Variant Server ARHGAP36_000038 1/10563 1/6728 0/3835
?/? c.948G>A r.(=) p.(=) g.130219031G>A Copied from the Exome Variant Server ARHGAP36_000039 1/10563 0/6728 1/3835
?/? c.955+42A>T r.(=) p.(=) g.130219080A>T Copied from the Exome Variant Server ARHGAP36_000040 1/10563 0/6728 1/3835
?/? c.956-11C>T r.(=) p.(=) g.130219551C>T Copied from the Exome Variant Server ARHGAP36_000041 3/10563 2/6728 1/3835
?/? c.1012C>T r.(?) p.(Pro338Ser) g.130219618C>T Copied from the Exome Variant Server ARHGAP36_000042 1/10563 1/6728 0/3835
?/? c.1046A>G r.(?) p.(Lys349Arg) g.130219652A>G Copied from the Exome Variant Server ARHGAP36_000043 1/10563 0/6728 1/3835
?/? c.1092T>C r.(=) p.(=) g.130219698T>C Copied from the Exome Variant Server ARHGAP36_000044 1/10563 0/6728 1/3835
?/? c.1104+13T>C r.(=) p.(=) g.130219723T>C Copied from the Exome Variant Server ARHGAP36_000045 2091/10563 761/6728 1330/3835
?/? c.1105-30G>A r.(=) p.(=) g.130219857G>A Copied from the Exome Variant Server ARHGAP36_000046 5/10563 1/6728 4/3835
?/? c.1105-9T>C r.(=) p.(=) g.130219878T>C Copied from the Exome Variant Server ARHGAP36_000047 1/10563 0/6728 1/3835
?/? c.1105G>A r.(?) p.(Val369Ile) g.130219887G>A Copied from the Exome Variant Server ARHGAP36_000048 1/10563 1/6728 0/3835
?/? c.1238A>G r.(?) p.(Asn413Ser) g.130220020A>G Copied from the Exome Variant Server ARHGAP36_000049 1/10563 1/6728 0/3835
?/? c.1246C>T r.(?) p.(Arg416Cys) g.130220028C>T Copied from the Exome Variant Server ARHGAP36_000050 1/10563 1/6728 0/3835
?/? c.1250C>T r.(?) p.(Ala417Val) g.130220032C>T Copied from the Exome Variant Server ARHGAP36_000051 1/10563 0/6728 1/3835
?/? c.1282-36T>C r.(=) p.(=) g.130220267T>C Copied from the Exome Variant Server ARHGAP36_000052 1/10563 0/6728 1/3835
?/? c.1282-30G>A r.(=) p.(=) g.130220273G>A Copied from the Exome Variant Server ARHGAP36_000053 1/10563 0/6728 1/3835
?/? c.1357C>T r.(?) p.(Arg453Cys) g.130220378C>T Copied from the Exome Variant Server ARHGAP36_000054 1/10563 1/6728 0/3835
?/? c.1380-42G>A r.(=) p.(=) g.130220491G>A Copied from the Exome Variant Server ARHGAP36_000055 1/10563 0/6728 1/3835
?/? c.1388G>T r.(?) p.(Arg463Leu) g.130220541G>T Copied from the Exome Variant Server ARHGAP36_000056 1/10563 1/6728 0/3835
?/? c.1486+10_1486+11insT r.(=) p.(=) g.130220649_130220650insT Copied from the Exome Variant Server ARHGAP36_000057 2/10205 2/6484 0/3721
?/? c.1486+41_1486+42insT r.(=) p.(=) g.130220680_130220681insT Copied from the Exome Variant Server ARHGAP36_000058 2/10205 2/6484 0/3721
?/? c.1487-18A>G r.(=) p.(=) g.130222584A>G Copied from the Exome Variant Server ARHGAP36_000059 7/10563 6/6728 1/3835
?/? c.1515C>T r.(=) p.(=) g.130222630C>T Copied from the Exome Variant Server ARHGAP36_000060 1/10563 0/6728 1/3835
?/? c.1520C>T r.(?) p.(Thr507Ile) g.130222635C>T Copied from the Exome Variant Server ARHGAP36_000061 2/10563 2/6728 0/3835
?/? c.1523C>T r.(?) p.(Ala508Val) g.130222638C>T Copied from the Exome Variant Server ARHGAP36_000062 1/10563 1/6728 0/3835
?/? c.1536C>T r.(=) p.(=) g.130222651C>T Copied from the Exome Variant Server ARHGAP36_000063 12/10563 12/6728 0/3835
?/? c.1550C>T r.(?) p.(Ala517Val) g.130222665C>T Copied from the Exome Variant Server ARHGAP36_000064 1/10563 1/6728 0/3835
?/? c.1568C>T r.(?) p.(Pro523Leu) g.130222683C>T Copied from the Exome Variant Server ARHGAP36_000065 1/10563 0/6728 1/3835
?/? c.1569G>A r.(=) p.(=) g.130222684G>A Copied from the Exome Variant Server ARHGAP36_000066 1/10563 0/6728 1/3835
?/? c.1574A>C r.(?) p.(Gln525Pro) g.130222689A>C Copied from the Exome Variant Server ARHGAP36_000067 1/10563 0/6728 1/3835
?/? c.1592G>A r.(?) p.(Arg531His) g.130222707G>A Copied from the Exome Variant Server ARHGAP36_000068 1/10563 1/6728 0/3835
?/? c.1600C>T r.(?) p.(Arg534Trp) g.130222715C>T Copied from the Exome Variant Server ARHGAP36_000069 1/10563 1/6728 0/3835
?/? c.1601G>T r.(?) p.(Arg534Leu) g.130222716G>T Copied from the Exome Variant Server ARHGAP36_000070 1/10563 0/6728 1/3835
?/? c.1623C>T r.(=) p.(=) g.130222738C>T Copied from the Exome Variant Server ARHGAP36_000071 1/10563 1/6728 0/3835
?/? c.*46G>A r.(=) p.(=) g.130222805G>A Copied from the Exome Variant Server ARHGAP36_000072 1/10563 1/6728 0/3835
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