Full data view for gene GSTCD

Information The variants shown are described using the NM_024751.2 transcript reference sequence.

69 entries on 1 page. Showing entries 1 - 69.
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Effect     

AscendingDNA change (cDNA)     

RNA change     

Protein     

DNA change (genomic) (hg19)     

Reference     

DB-ID     

Frequency     

Freq. EA     

Freq. AA     

Template     

Technique     

Disease     

Reference     

Remarks     

Panel size     

Owner     
?/? c.-21-7A>G r.(=) p.(=) g.106638743A>G Copied from the Exome Variant Server GSTCD_000001 1/12998 1/8600 0/4398 - - - - - - -
?/? c.-8A>G r.(=) p.(=) g.106638763A>G Copied from the Exome Variant Server GSTCD_000002 3/13002 3/8600 0/4402 - - - - - - -
?/? c.29A>G r.(?) p.(Glu10Gly) g.106638799A>G Copied from the Exome Variant Server GSTCD_000003 1/13006 1/8600 0/4406 - - - - - - -
?/? c.163G>A r.(?) p.(Glu55Lys) g.106638933G>A Copied from the Exome Variant Server GSTCD_000004 1/13006 0/8600 1/4406 - - - - - - -
?/? c.165+21A>G r.(=) p.(=) g.106638956A>G Copied from the Exome Variant Server GSTCD_000005 1/13006 0/8600 1/4406 - - - - - - -
?/? c.165+30T>C r.(=) p.(=) g.106638965T>C Copied from the Exome Variant Server GSTCD_000006 2/13006 1/8600 1/4406 - - - - - - -
?/? c.165+131A>G r.(=) p.(=) g.106639066A>G Copied from the Exome Variant Server GSTCD_000007 2/13006 0/8600 2/4406 - - - - - - -
?/? c.165+208G>C r.(=) p.(=) g.106639143G>C Copied from the Exome Variant Server GSTCD_000008 1/13006 1/8600 0/4406 - - - - - - -
?/? c.165+215_165+223del r.(=) p.(=) g.106639150_106639158del Copied from the Exome Variant Server GSTCD_000010 1/12520 0/8254 1/4266 - - - - - - -
?/? c.165+241T>A r.(=) p.(=) g.106639176T>A Copied from the Exome Variant Server GSTCD_000012 41/13006 40/8600 1/4406 - - - - - - -
?/? c.165+251C>A r.(=) p.(=) g.106639186C>A Copied from the Exome Variant Server GSTCD_000014 1/13006 0/8600 1/4406 - - - - - - -
?/? c.166-50T>C r.(=) p.(=) g.106640167T>C Copied from the Exome Variant Server GSTCD_000017 3/12350 3/8382 0/3968 - - - - - - -
?/? c.166-49A>G r.(=) p.(=) g.106640168A>G Copied from the Exome Variant Server GSTCD_000019 2/12388 0/8392 2/3996 - - - - - - -
?/? c.166-33C>A r.(=) p.(=) g.106640184C>A Copied from the Exome Variant Server GSTCD_000021 2159/12694 702/8510 1457/4184 - - - - - - -
?/? c.326G>A r.(?) p.(Arg109His) g.106640377G>A Copied from the Exome Variant Server GSTCD_000023 3/13006 2/8600 1/4406 - - - - - - -
?/? c.336G>A r.(=) p.(=) g.106640387G>A Copied from the Exome Variant Server GSTCD_000025 198/13006 0/8600 198/4406 - - - - - - -
?/? c.396C>A r.(?) p.(Ser132Arg) g.106640447C>A Copied from the Exome Variant Server GSTCD_000027 2/13006 2/8600 0/4406 - - - - - - -
?/? c.401T>G r.(?) p.(Val134Gly) g.106640452T>G Copied from the Exome Variant Server GSTCD_000029 3/13006 1/8600 2/4406 - - - - - - -
?/? c.411G>C r.(?) p.(Gln137His) g.106640462G>C Copied from the Exome Variant Server GSTCD_000009 1/13006 0/8600 1/4406 - - - - - - -
?/? c.451G>A r.(?) p.(Glu151Lys) g.106640502G>A Copied from the Exome Variant Server GSTCD_000011 2/13006 0/8600 2/4406 - - - - - - -
?/? c.510A>G r.(=) p.(=) g.106640561A>G Copied from the Exome Variant Server GSTCD_000013 1/13006 0/8600 1/4406 - - - - - - -
?/? c.525C>T r.(=) p.(=) g.106640576C>T Copied from the Exome Variant Server GSTCD_000015 1/13006 1/8600 0/4406 - - - - - - -
?/? c.543C>T r.(=) p.(=) g.106640594C>T Copied from the Exome Variant Server GSTCD_000016 1/13006 0/8600 1/4406 - - - - - - -
?/? c.544G>A r.(?) p.(Asp182Asn) g.106640595G>A Copied from the Exome Variant Server GSTCD_000018 8/13006 0/8600 8/4406 - - - - - - -
?/? c.553C>G r.(?) p.(Pro185Ala) g.106640604C>G Copied from the Exome Variant Server GSTCD_000020 1/13006 1/8600 0/4406 - - - - - - -
?/? c.580C>T r.(?) p.(Leu194Phe) g.106640631C>T Copied from the Exome Variant Server GSTCD_000022 4/13006 0/8600 4/4406 - - - - - - -
?/? c.633+32A>G r.(=) p.(=) g.106640716A>G Copied from the Exome Variant Server GSTCD_000024 1/13006 1/8600 0/4406 - - - - - - -
?/? c.753A>G r.(=) p.(=) g.106647855A>G Copied from the Exome Variant Server GSTCD_000026 1/13006 1/8600 0/4406 - - - - - - -
?/? c.885+50C>G r.(=) p.(=) g.106648037C>G Copied from the Exome Variant Server GSTCD_000028 1/12970 1/8588 0/4382 - - - - - - -
?/? c.886-38A>G r.(=) p.(=) g.106650525A>G Copied from the Exome Variant Server GSTCD_000030 61/13006 0/8600 61/4406 - - - - - - -
?/? c.892G>A r.(?) p.(Gly298Ser) g.106650569G>A Copied from the Exome Variant Server GSTCD_000031 1/13006 0/8600 1/4406 - - - - - - -
?/? c.954C>G r.(=) p.(=) g.106650631C>G Copied from the Exome Variant Server GSTCD_000032 1282/13006 50/8600 1232/4406 - - - - - - -
?/? c.959C>T r.(?) p.(Ala320Val) g.106650636C>T Copied from the Exome Variant Server GSTCD_000033 1/13006 1/8600 0/4406 - - - - - - -
?/? c.976G>A r.(?) p.(Glu326Lys) g.106650653G>A Copied from the Exome Variant Server GSTCD_000034 1/13006 1/8600 0/4406 - - - - - - -
?/? c.980-11G>A r.(=) p.(=) g.106744100G>A Copied from the Exome Variant Server GSTCD_000035 1/13006 0/8600 1/4406 - - - - - - -
?/? c.1095+13T>G r.(=) p.(=) g.106744239T>G Copied from the Exome Variant Server GSTCD_000036 3/13006 3/8600 0/4406 - - - - - - -
?/? c.1096-14_1096-11del r.(=) p.(=) g.106744374_106744377del Copied from the Exome Variant Server GSTCD_000037 61/12284 45/8166 16/4118 - - - - - - -
?/? c.1140+49T>G r.(=) p.(=) g.106744481T>G Copied from the Exome Variant Server GSTCD_000038 10/11850 0/8170 10/3680 - - - - - - -
?/? c.1140+52G>A r.(=) p.(=) g.106744484G>A Copied from the Exome Variant Server GSTCD_000039 1/6112 1/4186 0/1926 - - - - - - -
?/? c.1173A>G r.(=) p.(=) g.106746861A>G Copied from the Exome Variant Server GSTCD_000040 1/11728 1/8118 0/3610 - - - - - - -
?/? c.1178G>A r.(?) p.(Arg393His) g.106746866G>A Copied from the Exome Variant Server GSTCD_000041 1/11724 1/8114 0/3610 - - - - - - -
?/? c.1192A>G r.(?) p.(Ser398Gly) g.106746880A>G Copied from the Exome Variant Server GSTCD_000042 1/11728 1/8120 0/3608 - - - - - - -
?/? c.1203G>A r.(=) p.(=) g.106746891G>A Copied from the Exome Variant Server GSTCD_000043 1/11742 0/8132 1/3610 - - - - - - -
?/? c.1239G>A r.(?) p.(Met413Ile) g.106746927G>A Copied from the Exome Variant Server GSTCD_000044 53/11702 0/8112 53/3590 - - - - - - -
?/? c.1283C>T r.(?) p.(Ala428Val) g.106755631C>T Copied from the Exome Variant Server GSTCD_000045 2/12320 0/8366 2/3954 - - - - - - -
?/? c.1293G>A r.(=) p.(=) g.106755641G>A Copied from the Exome Variant Server GSTCD_000046 1/12334 1/8366 0/3968 - - - - - - -
?/? c.1297A>G r.(?) p.(Thr433Ala) g.106755645A>G Copied from the Exome Variant Server GSTCD_000047 1/12334 1/8366 0/3968 - - - - - - -
?/? c.1299A>G r.(=) p.(=) g.106755647A>G Copied from the Exome Variant Server GSTCD_000048 2/12326 2/8360 0/3966 - - - - - - -
?/? c.1320T>G r.(?) p.(Cys440Trp) g.106755668T>G Copied from the Exome Variant Server GSTCD_000049 1/12300 1/8338 0/3962 - - - - - - -
?/? c.1376A>T r.(?) p.(Asn459Ile) g.106755724A>T Copied from the Exome Variant Server GSTCD_000050 1/12102 0/8272 1/3830 - - - - - - -
?/? c.1379C>T r.(?) p.(Thr460Ile) g.106755727C>T Copied from the Exome Variant Server GSTCD_000051 1/12078 1/8264 0/3814 - - - - - - -
?/? c.1385A>G r.(?) p.(Lys462Arg) g.106755733A>G Copied from the Exome Variant Server GSTCD_000053 3/12016 3/8240 0/3776 - - - - - - -
?/? c.1403+36T>C r.(=) p.(=) g.106755787T>C Copied from the Exome Variant Server GSTCD_000055 1/11908 1/8196 0/3712 - - - - - - -
?/? c.1404-17del r.(=) p.(=) g.106758999del Copied from the Exome Variant Server GSTCD_000057 142/10992 110/7610 32/3382 - - - - - - -
?/? c.1404-11T>G r.(=) p.(=) g.106759005T>G Copied from the Exome Variant Server GSTCD_000059 1/11458 0/7966 1/3492 - - - - - - -
?/? c.1404-1_1404insT N/A N/A g.106759015_106759016insT Copied from the Exome Variant Server GSTCD_000061 1/11050 0/7648 1/3402 - - - - - - -
?/? c.1429T>C r.(?) p.(Tyr477His) g.106759041T>C Copied from the Exome Variant Server GSTCD_000063 1/11514 1/8008 0/3506 - - - - - - -
?/? c.1434+36A>G r.(=) p.(=) g.106759082A>G Copied from the Exome Variant Server GSTCD_000065 264/11496 7/8000 257/3496 - - - - - - -
?/? c.1435-16T>C r.(=) p.(=) g.106763206T>C Copied from the Exome Variant Server GSTCD_000067 1/11852 1/8174 0/3678 - - - - - - -
?/? c.1491A>G r.(=) p.(=) g.106763278A>G Copied from the Exome Variant Server GSTCD_000052 1/12054 1/8258 0/3796 - - - - - - -
?/? c.1518G>T r.(?) p.(Met506Ile) g.106766611G>T Copied from the Exome Variant Server GSTCD_000054 1/12316 0/8340 1/3976 - - - - - - -
?/? c.1537C>T r.(?) p.(Arg513*) g.106766630C>T Copied from the Exome Variant Server GSTCD_000056 1/12304 0/8354 1/3950 - - - - - - -
?/? c.1548T>C r.(=) p.(=) g.106766641T>C Copied from the Exome Variant Server GSTCD_000058 1/12256 1/8332 0/3924 - - - - - - -
?/? c.1570G>A r.(?) p.(Val524Ile) g.106766663G>A Copied from the Exome Variant Server GSTCD_000060 4/12206 3/8308 1/3898 - - - - - - -
?/? c.1618_1619del r.(?) p.(Met540Aspfs*9) g.106766711_106766712del Copied from the Exome Variant Server GSTCD_000062 1/11540 0/7896 1/3644 - - - - - - -
?/? c.1621A>T r.(?) p.(Ile541Phe) g.106766714A>T Copied from the Exome Variant Server GSTCD_000064 1/11996 0/8238 1/3758 - - - - - - -
?/? c.*13A>G r.(=) p.(=) g.106766747A>G Copied from the Exome Variant Server GSTCD_000066 1/11992 1/8232 0/3760 - - - - - - -
?/? c.*41C>T r.(=) p.(=) g.106766775C>T Copied from the Exome Variant Server GSTCD_000068 1/11998 1/8226 0/3772 - - - - - - -
?/? c.*42G>A r.(=) p.(=) g.106766776G>A Copied from the Exome Variant Server GSTCD_000069 8/12016 1/8236 7/3780 - - - - - - -
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