Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> PIK3CG

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000359195
Start 106868045:106868045(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.484G>A
AA Mutation p.Val162Ile(p.V162I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000359195
Start 106869094:106869094(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1533G>T
AA Mutation p.Glu511Asp(p.E511D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000359195
Start 106882124:106882124(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs746783339
CDS Mutation c.2546G>A
AA Mutation p.Arg849Gln(p.R849Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000359195
Start 106883060:106883060(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2657C>T
AA Mutation p.Thr886Met(p.T886M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000359195
Start 106869192:106869192(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1631G>A
AA Mutation p.Arg544Gln(p.R544Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000359195
Start 106867706:106867706(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.145C>T
AA Mutation p.Arg49Cys(p.R49C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000359195
Start 106867637:106867637(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.76C>T
AA Mutation p.Arg26Cys(p.R26C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000359195
Start 106869134:106869134(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1573C>A
AA Mutation p.His525Asn(p.H525N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000359195
Start 106867719:106867719(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs540366635
CDS Mutation c.158G>A
AA Mutation p.Ser53Asn(p.S53N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000359195
Start 106905140:106905140(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs376453517
CDS Mutation c.3062G>A
AA Mutation p.Arg1021His(p.R1021H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000359195
Start 106868446:106868446(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs112943477
CDS Mutation c.885C>G
AA Mutation p.His295Gln(p.H295Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000359195
Start 106868510:106868510(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs759136884
CDS Mutation c.949G>A
AA Mutation p.Glu317Lys(p.E317K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000359195
Start 106868381:106868381(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.820G>A
AA Mutation p.Val274Ile(p.V274I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000359195
Start 106867676:106867676(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.115C>A
AA Mutation p.Pro39Thr(p.P39T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000359195
Start 106868543:106868543(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs367672522
CDS Mutation c.982G>A
AA Mutation p.Asp328Asn(p.D328N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000359195
Start 106868990:106868990(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs138344795
CDS Mutation c.1429C>T
AA Mutation p.Arg477Cys(p.R477C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000359195
Start 106868516:106868516(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.955A>T
AA Mutation p.Arg319Trp(p.R319W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000359195
Start 106905232:106905232(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs765204428
CDS Mutation c.3154C>T
AA Mutation p.Arg1052Trp(p.R1052W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000359195
Start 106869224:106869224(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1663T>A
AA Mutation p.Leu555Met(p.L555M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000359195
Start 106882203:106882203(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2625A>C
AA Mutation p.Lys875Asn(p.K875N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000359195
Start 106905295:106905295(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3217G>A
AA Mutation p.Glu1073Lys(p.E1073K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000359195
Start 106883052:106883052(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2649A>C
AA Mutation p.Lys883Asn(p.K883N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000359195
Start 106867889:106867889(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.328T>C
AA Mutation p.Tyr110His(p.Y110H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000359195
Start 106868077:106868077(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.516G>T
AA Mutation p.Glu172Asp(p.E172D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence synonymous_variant
Transcription ID ENST00000359195
Start 106867891:106867891(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs374729346
CDS Mutation c.330C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 26
Mutation Consequence synonymous_variant
Transcription ID ENST00000359195
Start 106868957:106868957(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1396C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 27
Mutation Consequence synonymous_variant
Transcription ID ENST00000359195
Start 106868347:106868347(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs555666943
CDS Mutation c.786C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 28
Mutation Consequence synonymous_variant
Transcription ID ENST00000359195
Start 106883055:106883055(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs755002463
CDS Mutation c.2652C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 29
Mutation Consequence synonymous_variant
Transcription ID ENST00000359195
Start 106868566:106868566(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1005C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 30
Mutation Consequence synonymous_variant
Transcription ID ENST00000359195
Start 106879581:106879581(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs763798647
CDS Mutation c.2454C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 31
Mutation Consequence synonymous_variant
Transcription ID ENST00000359195
Start 106868053:106868053(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.492C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 32
Mutation Consequence synonymous_variant
Transcription ID ENST00000359195
Start 106869503:106869503(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1942C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 33
Mutation Consequence synonymous_variant
Transcription ID ENST00000359195
Start 106879647:106879647(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2520A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 34
Mutation Consequence synonymous_variant
Transcription ID ENST00000359195
Start 106868410:106868410(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs766973241
CDS Mutation c.849C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 35
Mutation Consequence synonymous_variant
Transcription ID ENST00000359195
Start 106868185:106868185(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs756654814
CDS Mutation c.624G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 36
Mutation Consequence synonymous_variant
Transcription ID ENST00000359195
Start 106905384:106905384(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3306C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 37
Mutation Consequence synonymous_variant
Transcription ID ENST00000359195
Start 106869232:106869232(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs267601222
CDS Mutation c.1671G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 38
Mutation Consequence stop_lost
Transcription ID ENST00000359195
Start 106905386:106905386(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3308A>C
AA Mutation p.Ter1103SerextTer10(p.*1103Sext*10)
Mutation Classification Nonstop_Mutation
Feature Type Transcript

Rectum Cancer: Gene >> PIK3CG

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000359195
Start 106868633:106868633(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs62001903
CDS Mutation c.1072G>A
AA Mutation p.Asp358Asn(p.D358N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000359195
Start 106905352:106905352(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3274C>A
AA Mutation p.Leu1092Ile(p.L1092I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000359195
Start 106867638:106867638(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.77G>A
AA Mutation p.Arg26His(p.R26H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000359195
Start 106868025:106868025(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.464C>T
AA Mutation p.Thr155Met(p.T155M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000359195
Start 106868276:106868276(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs754275924
CDS Mutation c.715G>A
AA Mutation p.Asp239Asn(p.D239N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000359195
Start 106872565:106872565(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2024G>A
AA Mutation p.Ser675Asn(p.S675N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000359195
Start 106872720:106872720(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs778461029
CDS Mutation c.2069G>T
AA Mutation p.Arg690Ile(p.R690I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000359195
Start 106886157:106886157(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs758101618
CDS Mutation c.2895C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000359195
Start 106867987:106867987(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.426G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000359195
Start 106883146:106883146(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2743delT
AA Mutation p.Ser915ProfsTer30(p.S915Pfs*30)
Mutation Classification Frame_Shift_Del
Feature Type Transcript