Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CAMTA1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000303635
Start 7664100:7664100(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1553G>A
AA Mutation p.Gly518Glu(p.G518E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000303635
Start 7663424:7663424(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.877C>T
AA Mutation p.Arg293Trp(p.R293W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000303635
Start 7664381:7664381(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1834C>T
AA Mutation p.Pro612Ser(p.P612S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000303635
Start 7664352:7664352(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs150582508
CDS Mutation c.1805C>T
AA Mutation p.Thr602Met(p.T602M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000303635
Start 7732455:7732455(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2922G>T
AA Mutation p.Gln974His(p.Q974H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000303635
Start 7663398:7663398(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767725186
CDS Mutation c.851G>T
AA Mutation p.Arg284Leu(p.R284L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000303635
Start 7664493:7664493(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs772421310
CDS Mutation c.1946C>T
AA Mutation p.Thr649Met(p.T649M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000303635
Start 7663841:7663841(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767458145
CDS Mutation c.1294G>A
AA Mutation p.Val432Ile(p.V432I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000303635
Start 7732595:7732595(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3062C>T
AA Mutation p.Ala1021Val(p.A1021V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000303635
Start 7738022:7738022(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3722C>T
AA Mutation p.Pro1241Leu(p.P1241L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000303635
Start 7665008:7665008(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2461C>T
AA Mutation p.Leu821Phe(p.L821F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000303635
Start 7737325:7737325(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs750477632
CDS Mutation c.3413C>T
AA Mutation p.Ser1138Leu(p.S1138L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000303635
Start 7640509:7640509(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs745719073
CDS Mutation c.620C>T
AA Mutation p.Ala207Val(p.A207V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000303635
Start 7664237:7664237(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1690G>A
AA Mutation p.Ala564Thr(p.A564T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000303635
Start 7671037:7671037(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2779G>T
AA Mutation p.Ala927Ser(p.A927S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000303635
Start 7664765:7664765(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs772482641
CDS Mutation c.2218G>A
AA Mutation p.Val740Met(p.V740M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000303635
Start 7640454:7640454(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs146417182
CDS Mutation c.565G>T
AA Mutation p.Gly189Cys(p.G189C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000303635
Start 7664882:7664882(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2335G>A
AA Mutation p.Asp779Asn(p.D779N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000303635
Start 7249538:7249538(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.350A>G
AA Mutation p.Tyr117Cys(p.Y117C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000303635
Start 7737971:7737971(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3671C>A
AA Mutation p.Pro1224His(p.P1224H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000303635
Start 7738302:7738302(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4002G>T
AA Mutation p.Gln1334His(p.Q1334H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000303635
Start 7664309:7664309(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs754356402
CDS Mutation c.1762G>A
AA Mutation p.Ala588Thr(p.A588T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000303635
Start 7640412:7640412(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.523G>A
AA Mutation p.Val175Ile(p.V175I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000303635
Start 7751292:7751292(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs759514197
CDS Mutation c.4783C>T
AA Mutation p.Arg1595Trp(p.R1595W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000303635
Start 7663870:7663870(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1323G>C
AA Mutation p.Lys441Asn(p.K441N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000303635
Start 7736386:7736386(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs752103947
CDS Mutation c.3109C>T
AA Mutation p.Arg1037Cys(p.R1037C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 27
Mutation Consequence synonymous_variant
Transcription ID ENST00000303635
Start 7091333:7091333(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.264G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 28
Mutation Consequence synonymous_variant
Transcription ID ENST00000303635
Start 7663873:7663873(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs141193119
CDS Mutation c.1326C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 29
Mutation Consequence synonymous_variant
Transcription ID ENST00000303635
Start 7664560:7664560(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2013C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 30
Mutation Consequence synonymous_variant
Transcription ID ENST00000303635
Start 7665115:7665115(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs374177752
CDS Mutation c.2568G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 31
Mutation Consequence synonymous_variant
Transcription ID ENST00000303635
Start 7664233:7664233(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1686G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 32
Mutation Consequence synonymous_variant
Transcription ID ENST00000303635
Start 7663513:7663513(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.966C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 33
Mutation Consequence synonymous_variant
Transcription ID ENST00000303635
Start 7664650:7664650(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2103C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 34
Mutation Consequence synonymous_variant
Transcription ID ENST00000303635
Start 7745953:7745953(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs775434446
CDS Mutation c.4479G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 35
Mutation Consequence synonymous_variant
Transcription ID ENST00000303635
Start 7664977:7664977(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs774395569
CDS Mutation c.2430G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 36
Mutation Consequence synonymous_variant
Transcription ID ENST00000303635
Start 7747778:7747778(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4686A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 37
Mutation Consequence synonymous_variant
Transcription ID ENST00000303635
Start 7746055:7746055(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4581T>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 38
Mutation Consequence synonymous_variant
Transcription ID ENST00000303635
Start 7737326:7737326(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs756637047
CDS Mutation c.3414G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 39
Mutation Consequence synonymous_variant
Transcription ID ENST00000303635
Start 7640492:7640492(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs757030542
CDS Mutation c.603C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 40
Mutation Consequence synonymous_variant
Transcription ID ENST00000303635
Start 7663819:7663819(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1272A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 41
Mutation Consequence synonymous_variant
Transcription ID ENST00000303635
Start 7736943:7736943(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs762946955
CDS Mutation c.3276G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 42
Mutation Consequence synonymous_variant
Transcription ID ENST00000303635
Start 7745926:7745926(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs139839670
CDS Mutation c.4452C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 43
Mutation Consequence frameshift_variant
Transcription ID ENST00000303635
Start 7751269:7751269(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.4767delA
AA Mutation p.Lys1589AsnfsTer33(p.K1589Nfs*33)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 44
Mutation Consequence stop_gained
Transcription ID ENST00000303635
Start 7640523:7640523(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.634G>T
AA Mutation p.Glu212Ter(p.E212*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 45
Mutation Consequence frameshift_variant
Transcription ID ENST00000303635
Start 6825138:6825139(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.167dupA
AA Mutation p.Leu57AlafsTer3(p.L57Afs*3)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 46
Mutation Consequence frameshift_variant
Transcription ID ENST00000303635
Start 7738075:7738076(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.3775_3776insTACAACT
AA Mutation p.Lys1259IlefsTer22(p.K1259Ifs*22)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript

Rectum Cancer: Gene >> CAMTA1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000303635
Start 7664429:7664429(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200762060
CDS Mutation c.1882G>A
AA Mutation p.Glu628Lys(p.E628K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000303635
Start 7744937:7744937(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4285G>T
AA Mutation p.Asp1429Tyr(p.D1429Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000303635
Start 7745951:7745951(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4477G>A
AA Mutation p.Ala1493Thr(p.A1493T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000303635
Start 7744978:7744978(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4326T>G
AA Mutation p.Ser1442Arg(p.S1442R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence stop_gained
Transcription ID ENST00000303635
Start 7747713:7747713(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4621C>T
AA Mutation p.Arg1541Ter(p.R1541*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript