All transcript variants in gene ARHGAP6

Information The variants shown are described using the NM_013427.2 transcript reference sequence.

141 entries on 2 pages. Showing entries 1 - 100.
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Effect     

AscendingDNA change (cDNA)     

RNA change     

Protein     

DNA change (genomic) (hg19)     

Reference     

DB-ID     

Frequency     

Freq. EA     

Freq. AA     
?/? c.-3G>A r.(=) p.(=) g.11682951C>T Copied from the Exome Variant Server ARHGAP6_000108 1/8273 0/5300 1/2973
?/? c.232C>T r.(?) p.(Arg78Cys) g.11682717G>A Copied from the Exome Variant Server ARHGAP6_000107 1/10019 0/6402 1/3617
?/? c.295C>T r.(?) p.(Leu99Phe) g.11682654G>A Copied from the Exome Variant Server ARHGAP6_000106 5/10514 0/6704 5/3810
?/? c.327G>A r.(=) p.(=) g.11682622C>T Copied from the Exome Variant Server ARHGAP6_000105 1/10553 1/6725 0/3828
?/? c.331_333del r.(?) p.(Glu111del) g.11682616_11682618del Copied from the Exome Variant Server ARHGAP6_000104 28/10196 12/6479 16/3717
?/? c.418C>A r.(?) p.(Pro140Thr) g.11682531G>T Copied from the Exome Variant Server ARHGAP6_000103 1/10562 0/6728 1/3834
?/? c.423T>G r.(=) p.(=) g.11682526A>C Copied from the Exome Variant Server ARHGAP6_000102 1/10562 1/6728 0/3834
?/? c.433G>C r.(?) p.(Gly145Arg) g.11682516C>G Copied from the Exome Variant Server ARHGAP6_000101 1/10561 0/6728 1/3833
?/? c.446G>A r.(?) p.(Ser149Asn) g.11682503C>T Copied from the Exome Variant Server ARHGAP6_000100 1/10561 1/6728 0/3833
?/? c.477C>T r.(=) p.(=) g.11682472G>A Copied from the Exome Variant Server ARHGAP6_000099 1/10562 0/6728 1/3834
?/? c.479G>T r.(?) p.(Gly160Val) g.11682470C>A Copied from the Exome Variant Server ARHGAP6_000098 2/10562 2/6728 0/3834
?/? c.484G>A r.(?) p.(Gly162Ser) g.11682465C>T Copied from the Exome Variant Server ARHGAP6_000097 3/10563 0/6728 3/3835
?/? c.486C>T r.(=) p.(=) g.11682463G>A Copied from the Exome Variant Server ARHGAP6_000096 1/10563 1/6728 0/3835
?/? c.496A>C r.(?) p.(Ile166Leu) g.11682453T>G Copied from the Exome Variant Server ARHGAP6_000095 1/10563 0/6728 1/3835
?/? c.570C>T r.(=) p.(=) g.11682379G>A Copied from the Exome Variant Server ARHGAP6_000094 189/10557 6/6727 183/3830
?/? c.585C>G r.(=) p.(=) g.11682364G>C Copied from the Exome Variant Server ARHGAP6_000093 1/10559 1/6728 0/3831
?/? c.589-45959G>T r.(=) p.(=) g.11318786C>A Copied from the Exome Variant Server AMELX_000033 1/3596 0/2387 1/1209
?/? c.589-45944G>A r.(=) p.(=) g.11318771C>T Copied from the Exome Variant Server AMELX_000032 1/10559 1/6724 0/3835
?/? c.589-45943C>T r.(=) p.(=) g.11318770G>A Copied from the Exome Variant Server AMELX_000031 10/10559 9/6724 1/3835
?/? c.589-45919C>T r.(=) p.(=) g.11318746G>A Copied from the Exome Variant Server AMELX_000030 2/10560 0/6725 2/3835
?/? c.589-45867A>G r.(=) p.(=) g.11318694T>C Copied from the Exome Variant Server AMELX_000029 1/10559 1/6724 0/3835
?/? c.589-45863A>G r.(=) p.(=) g.11318690T>C Copied from the Exome Variant Server AMELX_000028 1/10559 0/6724 1/3835
?/? c.589-44235G>T r.(?) p.(Pro180Gln) g.11317062C>A Copied from the Exome Variant Server AMELX_000027 1/10563 1/6728 0/3835
?/? c.589-44203G>A r.(=) p.(=) g.11317030C>T Copied from the Exome Variant Server AMELX_000026 1/10563 1/6728 0/3835
?/? c.589-44170C>T r.(=) p.(=) g.11316997G>A Copied from the Exome Variant Server AMELX_000025 15/10563 12/6728 3/3835
?/? c.589-44153G>T r.(?) p.(Pro153Thr) g.11316980C>A Copied from the Exome Variant Server AMELX_000024 2/10563 2/6728 0/3835
?/? c.589-44132C>A r.(?) p.(Val146Leu) g.11316959G>T Copied from the Exome Variant Server AMELX_000023 54/10563 0/6728 54/3835
?/? c.589-44062G>A r.(=) p.(=) g.11316889C>T Copied from the Exome Variant Server AMELX_000022 15/10563 2/6728 13/3835
?/? c.589-44003C>T r.(?) p.(Val103Ile) g.11316830G>A Copied from the Exome Variant Server AMELX_000021 1/10563 1/6728 0/3835
?/? c.589-43976C>T r.(?) p.(Val94Met) g.11316803G>A Copied from the Exome Variant Server AMELX_000020 2/10563 1/6728 1/3835
?/? c.589-43921C>A r.(=) p.(=) g.11316748G>T Copied from the Exome Variant Server AMELX_000019 1/10563 0/6728 1/3835
?/? c.589-43920G>T r.(?) p.(Pro75Gln) g.11316747C>A Copied from the Exome Variant Server AMELX_000018 1/10563 1/6728 0/3835
?/? c.589-43915G>A r.(=) p.(=) g.11316742C>T Copied from the Exome Variant Server AMELX_000017 2589/10563 1475/6728 1114/3835
?/? c.589-43898C>T r.(?) p.(Val68Met) g.11316725G>A Copied from the Exome Variant Server AMELX_000016 1/10563 0/6728 1/3835
?/? c.589-43858G>A r.(=) p.(=) g.11316685C>T Copied from the Exome Variant Server AMELX_000015 1/10563 1/6728 0/3835
?/? c.589-43845G>A r.(?) p.(Pro50Leu) g.11316672C>T Copied from the Exome Variant Server AMELX_000014 3/10563 0/6728 3/3835
?/? c.589-43824_589-43823del r.(=) p.(=) g.11316650_11316651del Copied from the Exome Variant Server AMELX_000013 2/10205 1/6484 1/3721
?/? c.589-43802G>A r.(=) p.(=) g.11316629C>T Copied from the Exome Variant Server AMELX_000012 1/10563 0/6728 1/3835
?/? c.589-43627G>A r.(=) p.(=) g.11316454C>T Copied from the Exome Variant Server AMELX_000011 5/3600 1/2391 4/1209
?/? c.589-43580G>A r.(=) p.(=) g.11316407C>T Copied from the Exome Variant Server AMELX_000010 6/10563 0/6728 6/3835
?/? c.589-43570C>T r.(=) p.(=) g.11316397G>A Copied from the Exome Variant Server AMELX_000009 1/10563 0/6728 1/3835
?/? c.589-43569G>A r.(?) p.(Pro48Leu) g.11316396C>T Copied from the Exome Variant Server AMELX_000008 1/10563 0/6728 1/3835
?/? c.589-43490_589-43489del r.(=) p.(=) g.11316316_11316317del Copied from the Exome Variant Server AMELX_000007 1/10205 1/6484 0/3721
?/? c.589-43448T>C r.(=) p.(=) g.11316275A>G Copied from the Exome Variant Server AMELX_000006 44/10563 41/6728 3/3835
?/? c.589-43378A>G r.(=) p.(=) g.11316205T>C Copied from the Exome Variant Server AMELX_000005 13/10563 12/6728 1/3835
?/? c.589-42095A>C r.(=) p.(=) g.11314922T>G Copied from the Exome Variant Server AMELX_000004 1/10563 0/6728 1/3835
?/? c.589-42023G>C r.(=) p.(=) g.11314850C>G Copied from the Exome Variant Server AMELX_000003 1/10563 0/6728 1/3835
?/? c.589-40200A>G r.(=) p.(=) g.11313027T>C Copied from the Exome Variant Server AMELX_000002 2703/3600 1658/2391 1045/1209
?/? c.589-40036T>G r.(=) p.(=) g.11312863A>C Copied from the Exome Variant Server AMELX_000001 44/10563 41/6728 3/3835
?/? c.589-35810T>C r.(=) p.(=) g.11308637A>G Copied from the Exome Variant Server ARHGAP6_000092 1/9359 1/6337 0/3022
?/? c.589-35742C>G r.(=) p.(=) g.11308569G>C Copied from the Exome Variant Server ARHGAP6_000091 1/9494 0/6386 1/3108
?/? c.589-35730G>A r.(=) p.(=) g.11308557C>T Copied from the Exome Variant Server ARHGAP6_000090 4/9512 0/6392 4/3120
?/? c.666G>A r.(=) p.(=) g.11272750C>T Copied from the Exome Variant Server ARHGAP6_000089 1/10563 1/6728 0/3835
?/? c.676C>T r.(?) p.(Arg226Trp) g.11272740G>A Copied from the Exome Variant Server ARHGAP6_000088 1/10563 0/6728 1/3835
?/? c.701A>G r.(?) p.(Gln234Arg) g.11272715T>C Copied from the Exome Variant Server ARHGAP6_000087 1/10563 0/6728 1/3835
?/? c.712G>A r.(?) p.(Asp238Asn) g.11272704C>T Copied from the Exome Variant Server ARHGAP6_000086 1/10563 1/6728 0/3835
?/? c.748+7C>T r.(=) p.(=) g.11272661G>A Copied from the Exome Variant Server ARHGAP6_000085 1/10563 0/6728 1/3835
?/? c.748+25C>T r.(=) p.(=) g.11272643G>A Copied from the Exome Variant Server ARHGAP6_000084 5/10563 4/6728 1/3835
?/? c.748+26G>A r.(=) p.(=) g.11272642C>T Copied from the Exome Variant Server ARHGAP6_000083 2/10563 1/6728 1/3835
?/? c.820+20A>T r.(=) p.(=) g.11215025T>A Copied from the Exome Variant Server ARHGAP6_000082 1/10550 0/6727 1/3823
?/? c.827T>G r.(?) p.(Ile276Ser) g.11207098A>C Copied from the Exome Variant Server ARHGAP6_000081 6/10563 6/6728 0/3835
?/? c.828C>T r.(=) p.(=) g.11207097G>A Copied from the Exome Variant Server ARHGAP6_000080 1/10563 0/6728 1/3835
?/? c.897C>T r.(=) p.(=) g.11207028G>A Copied from the Exome Variant Server ARHGAP6_000079 1/10563 1/6728 0/3835
?/? c.909C>T r.(=) p.(=) g.11207016G>A Copied from the Exome Variant Server ARHGAP6_000078 2/10563 2/6728 0/3835
?/? c.987C>G r.(?) p.(Ser329Arg) g.11206938G>C Copied from the Exome Variant Server ARHGAP6_000077 1/10563 0/6728 1/3835
?/? c.1035G>A r.(=) p.(=) g.11206890C>T Copied from the Exome Variant Server ARHGAP6_000076 4/10563 4/6728 0/3835
?/? c.1050G>A r.(=) p.(=) g.11206875C>T Copied from the Exome Variant Server ARHGAP6_000075 3/10563 3/6728 0/3835
?/? c.1077+9G>C r.(=) p.(=) g.11206839C>G Copied from the Exome Variant Server ARHGAP6_000074 1/10563 0/6728 1/3835
?/? c.1078-49G>C r.(=) p.(=) g.11204600C>G Copied from the Exome Variant Server ARHGAP6_000073 1/10562 1/6727 0/3835
?/? c.1078-20C>T r.(=) p.(=) g.11204571G>A Copied from the Exome Variant Server ARHGAP6_000072 4/10563 4/6728 0/3835
?/? c.1099A>G r.(?) p.(Ile367Val) g.11204530T>C Copied from the Exome Variant Server ARHGAP6_000071 1/10563 0/6728 1/3835
?/? c.1157C>T r.(?) p.(Pro386Leu) g.11204472G>A Copied from the Exome Variant Server ARHGAP6_000070 1/10563 1/6728 0/3835
?/? c.1178A>T r.(?) p.(Lys393Met) g.11204451T>A Copied from the Exome Variant Server ARHGAP6_000069 1/10563 1/6728 0/3835
?/? c.1179G>C r.(?) p.(Lys393Asn) g.11204450C>G Copied from the Exome Variant Server ARHGAP6_000068 1/10563 0/6728 1/3835
?/? c.1196A>C r.(?) p.(Lys399Thr) g.11204433T>G Copied from the Exome Variant Server ARHGAP6_000067 3/10563 0/6728 3/3835
?/? c.1239G>A r.(=) p.(=) g.11204390C>T Copied from the Exome Variant Server ARHGAP6_000066 69/10563 1/6728 68/3835
?/? c.1273+7A>G r.(=) p.(=) g.11204349T>C Copied from the Exome Variant Server ARHGAP6_000065 1/10563 1/6728 0/3835
?/? c.1273+38C>T r.(=) p.(=) g.11204318G>A Copied from the Exome Variant Server ARHGAP6_000064 1/10563 0/6728 1/3835
?/? c.1274-49G>A r.(=) p.(=) g.11200287C>T Copied from the Exome Variant Server ARHGAP6_000063 12/10563 0/6728 12/3835
?/? c.1274-26T>C r.(=) p.(=) g.11200264A>G Copied from the Exome Variant Server ARHGAP6_000062 1/10563 1/6728 0/3835
?/? c.1274-22C>G r.(=) p.(=) g.11200260G>C Copied from the Exome Variant Server ARHGAP6_000061 2956/10563 1590/6728 1366/3835
?/? c.1325G>A r.(?) p.(Arg442Lys) g.11200187C>T Copied from the Exome Variant Server ARHGAP6_000060 1/10563 1/6728 0/3835
?/? c.1329+46T>C r.(=) p.(=) g.11200137A>G Copied from the Exome Variant Server ARHGAP6_000059 1/10563 0/6728 1/3835
?/? c.1330-32T>C r.(=) p.(=) g.11197604A>G Copied from the Exome Variant Server ARHGAP6_000058 1/10563 1/6728 0/3835
?/? c.1330-19C>A r.(=) p.(=) g.11197591G>T Copied from the Exome Variant Server ARHGAP6_000057 1/10563 1/6728 0/3835
?/? c.1342T>C r.(?) p.(Phe448Leu) g.11197560A>G Copied from the Exome Variant Server ARHGAP6_000056 1/10563 0/6728 1/3835
?/? c.1428G>A r.(?) p.(Met476Ile) g.11197474C>T Copied from the Exome Variant Server ARHGAP6_000055 1/10563 1/6728 0/3835
?/? c.1468A>G r.(?) p.(Ile490Val) g.11197434T>C Copied from the Exome Variant Server ARHGAP6_000054 1/10563 0/6728 1/3835
?/? c.1480T>A r.(?) p.(Leu494Met) g.11197422A>T Copied from the Exome Variant Server ARHGAP6_000053 10/10563 0/6728 10/3835
?/? c.1481-44A>G r.(=) p.(=) g.11196412T>C Copied from the Exome Variant Server ARHGAP6_000052 20/10493 19/6681 1/3812
?/? c.1481-37C>T r.(=) p.(=) g.11196405G>A Copied from the Exome Variant Server ARHGAP6_000051 48/10515 43/6695 5/3820
?/? c.1551C>T r.(=) p.(=) g.11196298G>A Copied from the Exome Variant Server ARHGAP6_000050 1/10563 0/6728 1/3835
?/? c.1562G>A r.(?) p.(Arg521His) g.11196287C>T Copied from the Exome Variant Server ARHGAP6_000049 1/10563 0/6728 1/3835
?/? c.1578C>A r.(=) p.(=) g.11196271G>T Copied from the Exome Variant Server ARHGAP6_000048 171/10563 2/6728 169/3835
?/? c.1584C>T r.(=) p.(=) g.11196265G>A Copied from the Exome Variant Server ARHGAP6_000047 2/10563 0/6728 2/3835
?/? c.1599C>T r.(=) p.(=) g.11196250G>A Copied from the Exome Variant Server ARHGAP6_000046 5/10563 4/6728 1/3835
?/? c.1630-46T>C r.(=) p.(=) g.11187850A>G Copied from the Exome Variant Server ARHGAP6_000045 9/10563 8/6728 1/3835
?/? c.1630-45G>C r.(=) p.(=) g.11187849C>G Copied from the Exome Variant Server ARHGAP6_000044 1/10563 1/6728 0/3835
?/? c.1630-31A>G r.(=) p.(=) g.11187835T>C Copied from the Exome Variant Server ARHGAP6_000043 22/10563 1/6728 21/3835
?/? c.1724T>C r.(?) p.(Val575Ala) g.11187710A>G Copied from the Exome Variant Server ARHGAP6_000042 1/10563 0/6728 1/3835
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