Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CACNA1G

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000359106
Start 50599789:50599789(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3620G>A
AA Mutation p.Arg1207His(p.R1207H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000359106
Start 50599500:50599500(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3331A>T
AA Mutation p.Asn1111Tyr(p.N1111Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000359106
Start 50616371:50616371(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5008T>A
AA Mutation p.Phe1670Ile(p.F1670I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000359106
Start 50605902:50605902(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4301T>C
AA Mutation p.Phe1434Ser(p.F1434S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000359106
Start 50616278:50616278(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4915C>A
AA Mutation p.Leu1639Met(p.L1639M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000359106
Start 50596644:50596644(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs745410924
CDS Mutation c.3062C>A
AA Mutation p.Ala1021Asp(p.A1021D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000359106
Start 50569240:50569240(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.430A>G
AA Mutation p.Lys144Glu(p.K144E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000359106
Start 50604273:50604273(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4288G>A
AA Mutation p.Gly1430Arg(p.G1430R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000359106
Start 50605927:50605927(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4326G>T
AA Mutation p.Gln1442His(p.Q1442H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000359106
Start 50619801:50619801(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5900C>A
AA Mutation p.Pro1967His(p.P1967H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000359106
Start 50575646:50575646(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs370667544
CDS Mutation c.1244G>A
AA Mutation p.Arg415Gln(p.R415Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000359106
Start 50599788:50599788(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs775810943
CDS Mutation c.3619C>T
AA Mutation p.Arg1207Cys(p.R1207C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000359106
Start 50607978:50607978(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4664G>A
AA Mutation p.Arg1555Gln(p.R1555Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000359106
Start 50617511:50617511(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5095G>A
AA Mutation p.Ala1699Thr(p.A1699T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000359106
Start 50572639:50572639(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.832G>A
AA Mutation p.Gly278Ser(p.G278S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000359106
Start 50615411:50615411(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4810G>A
AA Mutation p.Val1604Ile(p.V1604I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000359106
Start 50591526:50591526(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2545C>T
AA Mutation p.Pro849Ser(p.P849S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000359106
Start 50572820:50572820(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1013A>G
AA Mutation p.Asp338Gly(p.D338G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000359106
Start 50618674:50618674(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5447A>G
AA Mutation p.Asp1816Gly(p.D1816G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000359106
Start 50596623:50596623(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3041G>T
AA Mutation p.Gly1014Val(p.G1014V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000359106
Start 50569794:50569794(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.577C>T
AA Mutation p.Arg193Trp(p.R193W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000359106
Start 50571952:50571952(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.661G>A
AA Mutation p.Val221Ile(p.V221I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000359106
Start 50576050:50576050(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs748354117
CDS Mutation c.1648G>A
AA Mutation p.Ala550Thr(p.A550T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000359106
Start 50600738:50600738(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768623076
CDS Mutation c.3703C>T
AA Mutation p.Arg1235Trp(p.R1235W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000359106
Start 50569749:50569749(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.532G>T
AA Mutation p.Ala178Ser(p.A178S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000359106
Start 50596597:50596597(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3015C>A
AA Mutation p.Phe1005Leu(p.F1005L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000359106
Start 50599555:50599555(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3386G>A
AA Mutation p.Arg1129Gln(p.R1129Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 28
Mutation Consequence missense_variant
Transcription ID ENST00000359106
Start 50590552:50590552(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2383C>A
AA Mutation p.Leu795Ile(p.L795I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 29
Mutation Consequence missense_variant
Transcription ID ENST00000359106
Start 50626110:50626110(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs771907755
CDS Mutation c.6493C>T
AA Mutation p.Arg2165Trp(p.R2165W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 30
Mutation Consequence missense_variant
Transcription ID ENST00000359106
Start 50626169:50626169(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6552C>G
AA Mutation p.His2184Gln(p.H2184Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 31
Mutation Consequence missense_variant
Transcription ID ENST00000359106
Start 50626170:50626170(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6553A>C
AA Mutation p.Ser2185Arg(p.S2185R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 32
Mutation Consequence missense_variant
Transcription ID ENST00000359106
Start 50626504:50626504(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6887G>A
AA Mutation p.Gly2296Glu(p.G2296E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 33
Mutation Consequence missense_variant
Transcription ID ENST00000359106
Start 50616365:50616365(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5002C>T
AA Mutation p.Arg1668Cys(p.R1668C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 34
Mutation Consequence missense_variant
Transcription ID ENST00000359106
Start 50590584:50590584(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2415T>G
AA Mutation p.Asn805Lys(p.N805K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 35
Mutation Consequence missense_variant
Transcription ID ENST00000359106
Start 50590476:50590476(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2307G>T
AA Mutation p.Glu769Asp(p.E769D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 36
Mutation Consequence missense_variant
Transcription ID ENST00000359106
Start 50626518:50626518(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs374573766
CDS Mutation c.6901C>T
AA Mutation p.Arg2301Trp(p.R2301W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 37
Mutation Consequence synonymous_variant
Transcription ID ENST00000359106
Start 50607967:50607967(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4653G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 38
Mutation Consequence synonymous_variant
Transcription ID ENST00000359106
Start 50618969:50618969(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200604758
CDS Mutation c.5742C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 39
Mutation Consequence synonymous_variant
Transcription ID ENST00000359106
Start 50571915:50571915(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.624G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 40
Mutation Consequence synonymous_variant
Transcription ID ENST00000359106
Start 50578411:50578411(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2148G>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 41
Mutation Consequence synonymous_variant
Transcription ID ENST00000359106
Start 50618846:50618846(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5619G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 42
Mutation Consequence synonymous_variant
Transcription ID ENST00000359106
Start 50575902:50575902(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1500C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 43
Mutation Consequence synonymous_variant
Transcription ID ENST00000359106
Start 50607979:50607979(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4665G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 44
Mutation Consequence synonymous_variant
Transcription ID ENST00000359106
Start 50573071:50573071(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1098T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 45
Mutation Consequence synonymous_variant
Transcription ID ENST00000359106
Start 50568948:50568948(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs529908416
CDS Mutation c.321C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 46
Mutation Consequence synonymous_variant
Transcription ID ENST00000359106
Start 50626214:50626214(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6597C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 47
Mutation Consequence synonymous_variant
Transcription ID ENST00000359106
Start 50569293:50569293(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs372851469
CDS Mutation c.483C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 48
Mutation Consequence synonymous_variant
Transcription ID ENST00000359106
Start 50592032:50592032(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs536992411
CDS Mutation c.2850C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 49
Mutation Consequence synonymous_variant
Transcription ID ENST00000359106
Start 50618747:50618747(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs770082668
CDS Mutation c.5520C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 50
Mutation Consequence synonymous_variant
Transcription ID ENST00000359106
Start 50572563:50572563(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs373642146
CDS Mutation c.756C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 51
Mutation Consequence synonymous_variant
Transcription ID ENST00000359106
Start 50575611:50575611(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1209G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 52
Mutation Consequence synonymous_variant
Transcription ID ENST00000359106
Start 50618241:50618241(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5325C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 53
Mutation Consequence synonymous_variant
Transcription ID ENST00000359106
Start 50624514:50624514(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6384G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 54
Mutation Consequence synonymous_variant
Transcription ID ENST00000359106
Start 50575590:50575590(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201089692
CDS Mutation c.1188G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 55
Mutation Consequence frameshift_variant
Transcription ID ENST00000359106
Start 50575943:50575943(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1546delC
AA Mutation p.Arg516GlyfsTer48(p.R516Gfs*48)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 56
Mutation Consequence frameshift_variant
Transcription ID ENST00000359106
Start 50607978:50607978(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.4666delG
AA Mutation p.Glu1556ArgfsTer15(p.E1556Rfs*15)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 57
Mutation Consequence frameshift_variant
Transcription ID ENST00000359106
Start 50626559:50626559(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.6948delC
AA Mutation p.Glu2317ArgfsTer47(p.E2317Rfs*47)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 58
Mutation Consequence stop_gained
Transcription ID ENST00000359106
Start 50600756:50600756(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3721C>T
AA Mutation p.Arg1241Ter(p.R1241*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 59
Mutation Consequence frameshift_variant
Transcription ID ENST00000359106
Start 50626502:50626503(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.6891dupG
AA Mutation p.Pro2298AlafsTer13(p.P2298Afs*13)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 60
Mutation Consequence frameshift_variant
Transcription ID ENST00000359106
Start 50576035:50576036(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.1640dupC
AA Mutation p.Gly548TrpfsTer31(p.G548Wfs*31)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript

Rectum Cancer: Gene >> CACNA1G

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000359106
Start 50601148:50601148(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs376210592
CDS Mutation c.3889C>T
AA Mutation p.Arg1297Cys(p.R1297C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000359106
Start 50572660:50572660(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.853G>A
AA Mutation p.Val285Met(p.V285M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000359106
Start 50600787:50600787(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3752G>A
AA Mutation p.Arg1251Gln(p.R1251Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000359106
Start 50618306:50618306(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5390G>C
AA Mutation p.Arg1797Pro(p.R1797P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000359106
Start 50609931:50609931(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs780560019
CDS Mutation c.4755G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000359106
Start 50572023:50572023(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs766932544
CDS Mutation c.732T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000359106
Start 50616328:50616328(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4965C>A
Mutation Classification Silent
Feature Type Transcript