All transcript variants in gene RASGRP2

Information The variants shown are described using the NM_153819.1 transcript reference sequence.

128 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.-49G>A r.(=) p.(=) g.64510387C>T Copied from the Exome Variant Server RASGRP2_000128 2/12320 2/8096 0/4224
?/? c.17A>G r.(?) p.(Asp6Gly) g.64510322T>C Copied from the Exome Variant Server RASGRP2_000127 6/12966 6/8578 0/4388
?/? c.19C>T r.(=) p.(=) g.64510320G>A Copied from the Exome Variant Server RASGRP2_000126 89/12968 7/8578 82/4390
?/? c.73+16G>A r.(=) p.(=) g.64510250C>T Copied from the Exome Variant Server RASGRP2_000125 267/12960 63/8572 204/4388
?/? c.73+40C>T r.(=) p.(=) g.64510226G>A Copied from the Exome Variant Server RASGRP2_000124 13/12950 0/8578 13/4372
?/? c.73+42C>T r.(=) p.(=) g.64510224G>A Copied from the Exome Variant Server RASGRP2_000123 1/12950 1/8578 0/4372
?/? c.153G>A r.(=) p.(=) g.64509505C>T Copied from the Exome Variant Server RASGRP2_000122 1/12996 1/8594 0/4402
?/? c.154C>T r.(=) p.(=) g.64509504G>A Copied from the Exome Variant Server RASGRP2_000121 108/12996 2/8594 106/4402
?/? c.176+30_176+31insC r.(=) p.(=) g.64509451_64509452insG Copied from the Exome Variant Server RASGRP2_000120 130/12360 84/8166 46/4194
?/? c.176+44A>G r.(=) p.(=) g.64509438T>C Copied from the Exome Variant Server RASGRP2_000118 274/12978 69/8588 205/4390
?/? c.195G>A r.(=) p.(=) g.64508955C>T Copied from the Exome Variant Server RASGRP2_000116 3/12984 3/8584 0/4400
?/? c.198C>G r.(?) p.(Asp66Glu) g.64508952G>C Copied from the Exome Variant Server RASGRP2_000114 1/12986 0/8586 1/4400
?/? c.239+31C>T r.(=) p.(=) g.64508880G>A Copied from the Exome Variant Server RASGRP2_000119 1/12922 1/8556 0/4366
?/? c.240-44A>G r.(=) p.(=) g.64508595T>C Copied from the Exome Variant Server RASGRP2_000117 3/12996 3/8594 0/4402
?/? c.240-27A>G r.(=) p.(=) g.64508578T>C Copied from the Exome Variant Server RASGRP2_000115 5/12994 1/8594 4/4400
?/? c.240-13C>T r.(=) p.(=) g.64508564G>A Copied from the Exome Variant Server RASGRP2_000113 2/12994 2/8594 0/4400
?/? c.240-11C>T r.(=) p.(=) g.64508562G>A Copied from the Exome Variant Server RASGRP2_000112 2/12994 1/8594 1/4400
?/? c.240-7C>T r.(=) p.(=) g.64508558G>A Copied from the Exome Variant Server RASGRP2_000111 1/12994 1/8594 0/4400
?/? c.240-6C>T r.(=) p.(=) g.64508557G>A Copied from the Exome Variant Server RASGRP2_000110 1/12994 0/8594 1/4400
?/? c.253G>A r.(?) p.(Ala85Thr) g.64508538C>T Copied from the Exome Variant Server RASGRP2_000109 3/12996 2/8594 1/4402
?/? c.264G>A r.(=) p.(=) g.64508527C>T Copied from the Exome Variant Server RASGRP2_000108 1/12996 0/8594 1/4402
?/? c.279C>T r.(=) p.(=) g.64508512G>A Copied from the Exome Variant Server RASGRP2_000107 2/12996 0/8594 2/4402
?/? c.370G>A r.(?) p.(Val124Ile) g.64508421C>T Copied from the Exome Variant Server RASGRP2_000106 1/12996 1/8594 0/4402
?/? c.371+5G>A r.spl? p.? g.64508415C>T Copied from the Exome Variant Server RASGRP2_000105 2/12996 2/8594 0/4402
?/? c.371+7G>T r.(=) p.(=) g.64508413C>A Copied from the Exome Variant Server RASGRP2_000104 9/12996 8/8594 1/4402
?/? c.371+32del r.(=) p.(=) g.64508388del Copied from the Exome Variant Server RASGRP2_000103 46/12518 34/8254 12/4264
?/? c.372-45T>G r.(=) p.(=) g.64507680A>C Copied from the Exome Variant Server RASGRP2_000102 11745/12996 8582/8594 3163/4402
?/? c.372-40C>T r.(=) p.(=) g.64507675G>A Copied from the Exome Variant Server RASGRP2_000101 1/12996 1/8594 0/4402
?/? c.391C>T r.(?) p.(Arg131Trp) g.64507616G>A Copied from the Exome Variant Server RASGRP2_000100 1/12996 1/8594 0/4402
?/? c.439T>G r.(?) p.(Ser147Ala) g.64507568A>C Copied from the Exome Variant Server RASGRP2_000099 1/12996 0/8594 1/4402
?/? c.489C>T r.(=) p.(=) g.64507518G>A Copied from the Exome Variant Server RASGRP2_000098 25/12996 0/8594 25/4402
?/? c.503G>A r.(?) p.(Arg168His) g.64507504C>T Copied from the Exome Variant Server RASGRP2_000097 5/12996 1/8594 4/4402
?/? c.511T>C r.(?) p.(Cys171Arg) g.64507496A>G Copied from the Exome Variant Server RASGRP2_000096 2/12996 1/8594 1/4402
?/? c.522+8C>T r.(=) p.(=) g.64507477G>A Copied from the Exome Variant Server RASGRP2_000095 405/12996 370/8594 35/4402
?/? c.522+25_522+26del r.(=) p.(=) g.64507459_64507460del Copied from the Exome Variant Server RASGRP2_000094 1/12518 1/8254 0/4264
?/? c.522+34A>G r.(=) p.(=) g.64507451T>C Copied from the Exome Variant Server RASGRP2_000093 1/12996 1/8594 0/4402
?/? c.523-35C>T r.(=) p.(=) g.64507316G>A Copied from the Exome Variant Server RASGRP2_000092 264/12994 247/8592 17/4402
?/? c.523-34A>G r.(=) p.(=) g.64507315T>C Copied from the Exome Variant Server RASGRP2_000091 11745/12994 8580/8592 3165/4402
?/? c.573C>T r.(=) p.(=) g.64507231G>A Copied from the Exome Variant Server RASGRP2_000090 2/12996 0/8594 2/4402
?/? c.653C>T r.(?) p.(Pro218Leu) g.64507151G>A Copied from the Exome Variant Server RASGRP2_000089 1/12996 1/8594 0/4402
?/? c.663C>T r.(=) p.(=) g.64507141G>A Copied from the Exome Variant Server RASGRP2_000088 1/12996 1/8594 0/4402
?/? c.682G>A r.(?) p.(Val228Ile) g.64507122C>T Copied from the Exome Variant Server RASGRP2_000087 1/12996 1/8594 0/4402
?/? c.693G>A r.(=) p.(=) g.64507111C>T Copied from the Exome Variant Server RASGRP2_000086 1/12996 1/8594 0/4402
?/? c.696+20G>A r.(=) p.(=) g.64507088C>T Copied from the Exome Variant Server RASGRP2_000085 1/12996 0/8594 1/4402
?/? c.697-48G>A r.(=) p.(=) g.64506996C>T Copied from the Exome Variant Server RASGRP2_000084 1/12996 0/8594 1/4402
?/? c.697-29C>T r.(=) p.(=) g.64506977G>A Copied from the Exome Variant Server RASGRP2_000083 1/12996 0/8594 1/4402
?/? c.697-20C>T r.(=) p.(=) g.64506968G>A Copied from the Exome Variant Server RASGRP2_000082 1/12996 0/8594 1/4402
?/? c.725C>T r.(?) p.(Thr242Met) g.64506920G>A Copied from the Exome Variant Server RASGRP2_000081 1/12996 1/8594 0/4402
?/? c.767C>G r.(?) p.(Ser256Cys) g.64506878G>C Copied from the Exome Variant Server RASGRP2_000080 1/12996 1/8594 0/4402
?/? c.792C>T r.(=) p.(=) g.64506853G>A Copied from the Exome Variant Server RASGRP2_000079 1/12996 1/8594 0/4402
?/? c.813+7G>A r.(=) p.(=) g.64506825C>T Copied from the Exome Variant Server RASGRP2_000078 6/12996 0/8594 6/4402
?/? c.813+24G>A r.(=) p.(=) g.64506808C>T Copied from the Exome Variant Server RASGRP2_000077 1/12996 0/8594 1/4402
?/? c.814-28G>C r.(=) p.(=) g.64504534C>G Copied from the Exome Variant Server RASGRP2_000076 1/12994 1/8594 0/4400
?/? c.814-6C>T r.(=) p.(=) g.64504512G>A Copied from the Exome Variant Server RASGRP2_000075 5/12994 5/8594 0/4400
?/? c.842C>T r.(?) p.(Thr281Met) g.64504478G>A Copied from the Exome Variant Server RASGRP2_000074 1/12996 1/8594 0/4402
?/? c.846G>A r.(=) p.(=) g.64504474C>T Copied from the Exome Variant Server RASGRP2_000073 2/12996 0/8594 2/4402
?/? c.889G>A r.(?) p.(Val297Met) g.64504431C>T Copied from the Exome Variant Server RASGRP2_000072 1/12996 0/8594 1/4402
?/? c.898C>T r.(?) p.(Arg300Cys) g.64504422G>A Copied from the Exome Variant Server RASGRP2_000071 1/12996 1/8594 0/4402
?/? c.954G>C r.(=) p.(=) g.64504366C>G Copied from the Exome Variant Server RASGRP2_000070 1/12994 1/8592 0/4402
?/? c.965T>G r.(?) p.(Leu322Arg) g.64504355A>C Copied from the Exome Variant Server RASGRP2_000068 1/12994 1/8592 0/4402
?/? c.982C>T r.(?) p.(Arg328Trp) g.64504338G>A Copied from the Exome Variant Server RASGRP2_000066 1/12994 1/8592 0/4402
?/? c.989A>G r.(?) p.(Asn330Ser) g.64504331T>C Copied from the Exome Variant Server RASGRP2_000064 1/12994 0/8592 1/4402
?/? c.991G>A r.(?) p.(Gly331Arg) g.64504329C>T Copied from the Exome Variant Server RASGRP2_000069 3/12996 3/8594 0/4402
?/? c.999G>A r.(=) p.(=) g.64504321C>T Copied from the Exome Variant Server RASGRP2_000067 6/12996 6/8594 0/4402
?/? c.1020C>T r.(=) p.(=) g.64504300G>A Copied from the Exome Variant Server RASGRP2_000065 1/12996 1/8594 0/4402
?/? c.1074C>T r.(=) p.(=) g.64504246G>A Copied from the Exome Variant Server RASGRP2_000063 3/12978 2/8584 1/4394
?/? c.1096-44T>C r.(=) p.(=) g.64503496A>G Copied from the Exome Variant Server RASGRP2_000062 12516/12996 8587/8594 3929/4402
?/? c.1096-39G>T r.(=) p.(=) g.64503491C>A Copied from the Exome Variant Server RASGRP2_000061 1/12996 1/8594 0/4402
?/? c.1096-38C>T r.(=) p.(=) g.64503490G>A Copied from the Exome Variant Server RASGRP2_000060 1/12996 0/8594 1/4402
?/? c.1096-33G>A r.(=) p.(=) g.64503485C>T Copied from the Exome Variant Server RASGRP2_000059 1/12996 1/8594 0/4402
?/? c.1096-24G>C r.(=) p.(=) g.64503476C>G Copied from the Exome Variant Server RASGRP2_000058 2/12996 0/8594 2/4402
?/? c.1118C>A r.(?) p.(Thr373Lys) g.64503430G>T Copied from the Exome Variant Server RASGRP2_000057 1/12996 0/8594 1/4402
?/? c.1157C>T r.(?) p.(Pro386Leu) g.64503391G>A Copied from the Exome Variant Server RASGRP2_000056 3/12996 2/8594 1/4402
?/? c.1158G>A r.(=) p.(=) g.64503390C>T Copied from the Exome Variant Server RASGRP2_000055 3/12996 3/8594 0/4402
?/? c.1173+8G>A r.(=) p.(=) g.64503367C>T Copied from the Exome Variant Server RASGRP2_000054 11/12996 0/8594 11/4402
?/? c.1173+12C>T r.(=) p.(=) g.64503363G>A Copied from the Exome Variant Server RASGRP2_000053 1759/12996 837/8594 922/4402
?/? c.1173+21C>A r.(=) p.(=) g.64503354G>T Copied from the Exome Variant Server RASGRP2_000052 1/12996 1/8594 0/4402
?/? c.1173+38C>G r.(=) p.(=) g.64503337G>C Copied from the Exome Variant Server RASGRP2_000051 2/12996 2/8594 0/4402
?/? c.1174-52C>T r.(=) p.(=) g.64503188G>A Copied from the Exome Variant Server RASGRP2_000050 2/7266 0/4614 2/2652
?/? c.1174-43T>C r.(=) p.(=) g.64503179A>G Copied from the Exome Variant Server RASGRP2_000049 11748/12950 8556/8568 3192/4382
?/? c.1174-15C>T r.(=) p.(=) g.64503151G>A Copied from the Exome Variant Server RASGRP2_000048 3/12980 0/8586 3/4394
?/? c.1214C>T r.(?) p.(Pro405Leu) g.64503096G>A Copied from the Exome Variant Server RASGRP2_000047 5/12994 0/8592 5/4402
?/? c.1246C>T r.(?) p.(Pro416Ser) g.64503064G>A Copied from the Exome Variant Server RASGRP2_000046 1/12996 0/8594 1/4402
?/? c.1266C>T r.(=) p.(=) g.64503044G>A Copied from the Exome Variant Server RASGRP2_000045 1/12996 0/8594 1/4402
?/? c.1267G>A r.(?) p.(Val423Met) g.64503043C>T Copied from the Exome Variant Server RASGRP2_000044 6/12996 1/8594 5/4402
?/? c.1296+12C>T r.(=) p.(=) g.64503002G>A Copied from the Exome Variant Server RASGRP2_000043 1/12996 1/8594 0/4402
?/? c.1297-16C>T r.(=) p.(=) g.64502715G>A Copied from the Exome Variant Server RASGRP2_000042 2/12996 2/8594 0/4402
?/? c.1306C>T r.(?) p.(Arg436Trp) g.64502690G>A Copied from the Exome Variant Server RASGRP2_000041 1/12996 1/8594 0/4402
?/? c.1307G>A r.(?) p.(Arg436Gln) g.64502689C>T Copied from the Exome Variant Server RASGRP2_000040 1/12996 1/8594 0/4402
?/? c.1320C>T r.(=) p.(=) g.64502676G>A Copied from the Exome Variant Server RASGRP2_000039 1/12996 1/8594 0/4402
?/? c.1335C>T r.(=) p.(=) g.64502661G>A Copied from the Exome Variant Server RASGRP2_000038 1/12996 1/8594 0/4402
?/? c.1339T>C r.(?) p.(Ser447Pro) g.64502657A>G Copied from the Exome Variant Server RASGRP2_000037 1/12996 0/8594 1/4402
?/? c.1363C>T r.(?) p.(Arg455Cys) g.64502633G>A Copied from the Exome Variant Server RASGRP2_000036 2/12996 2/8594 0/4402
?/? c.1386C>T r.(=) p.(=) g.64502610G>A Copied from the Exome Variant Server RASGRP2_000035 1/12996 1/8594 0/4402
?/? c.1388C>A r.(?) p.(Ala463Asp) g.64502608G>T Copied from the Exome Variant Server RASGRP2_000034 1/12996 1/8594 0/4402
?/? c.1401C>T r.(=) p.(=) g.64502595G>A Copied from the Exome Variant Server RASGRP2_000033 1/12996 0/8594 1/4402
?/? c.1412+25G>A r.(=) p.(=) g.64502559C>T Copied from the Exome Variant Server RASGRP2_000032 1/12996 1/8594 0/4402
?/? c.1413-44T>A r.(=) p.(=) g.64497710A>T Copied from the Exome Variant Server RASGRP2_000031 2/11380 2/7460 0/3920
?/? c.1413-14G>A r.(=) p.(=) g.64497680C>T Copied from the Exome Variant Server RASGRP2_000030 1/11790 1/7762 0/4028
?/? c.1413-3C>T r.spl? p.? g.64497669G>A Copied from the Exome Variant Server RASGRP2_000029 1/11894 0/7834 1/4060
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