Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> PCDH10

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000264360
Start 133163253:133163253(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747022854
CDS Mutation c.3074C>T
AA Mutation p.Thr1025Met(p.T1025M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000264360
Start 133151389:133151389(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1249A>G
AA Mutation p.Thr417Ala(p.T417A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000264360
Start 133190143:133190143(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3106C>T
AA Mutation p.Arg1036Trp(p.R1036W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000264360
Start 133152137:133152137(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1997C>T
AA Mutation p.Pro666Leu(p.P666L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000264360
Start 133152124:133152124(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1984G>T
AA Mutation p.Asp662Tyr(p.D662Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000264360
Start 133163088:133163088(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs571561006
CDS Mutation c.2909G>A
AA Mutation p.Arg970His(p.R970H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000264360
Start 133151326:133151326(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1186G>A
AA Mutation p.Glu396Lys(p.E396K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000264360
Start 133152443:133152443(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2303C>T
AA Mutation p.Ser768Leu(p.S768L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000264360
Start 133152355:133152355(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2215C>T
AA Mutation p.Arg739Cys(p.R739C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000264360
Start 133163259:133163259(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3080C>T
AA Mutation p.Ala1027Val(p.A1027V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000264360
Start 133151984:133151984(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1844G>A
AA Mutation p.Arg615Gln(p.R615Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000264360
Start 133150182:133150182(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.42A>C
AA Mutation p.Glu14Asp(p.E14D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000264360
Start 133150724:133150724(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.584C>T
AA Mutation p.Ala195Val(p.A195V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000264360
Start 133151800:133151800(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1660C>A
AA Mutation p.Leu554Met(p.L554M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000264360
Start 133152724:133152724(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs769806730
CDS Mutation c.2584G>A
AA Mutation p.Asp862Asn(p.D862N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000264360
Start 133163079:133163079(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2900C>T
AA Mutation p.Ala967Val(p.A967V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000264360
Start 133151252:133151252(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1112C>T
AA Mutation p.Ala371Val(p.A371V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000264360
Start 133151620:133151620(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1480G>A
AA Mutation p.Ala494Thr(p.A494T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000264360
Start 133151522:133151522(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1382C>T
AA Mutation p.Pro461Leu(p.P461L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000264360
Start 133151537:133151537(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1397C>T
AA Mutation p.Pro466Leu(p.P466L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000264360
Start 133152538:133152538(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2398G>A
AA Mutation p.Ala800Thr(p.A800T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000264360
Start 133151122:133151122(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.982G>A
AA Mutation p.Val328Met(p.V328M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000264360
Start 133150443:133150443(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.303C>G
AA Mutation p.Asn101Lys(p.N101K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000264360
Start 133150369:133150369(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.229G>A
AA Mutation p.Glu77Lys(p.E77K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000264360
Start 133151734:133151734(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1594G>A
AA Mutation p.Asp532Asn(p.D532N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000264360
Start 133151021:133151021(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.881C>T
AA Mutation p.Ser294Leu(p.S294L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000264360
Start 133152741:133152741(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2601C>G
AA Mutation p.Ile867Met(p.I867M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 28
Mutation Consequence missense_variant
Transcription ID ENST00000264360
Start 133151089:133151089(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.949G>A
AA Mutation p.Asp317Asn(p.D317N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 29
Mutation Consequence missense_variant
Transcription ID ENST00000264360
Start 133162994:133162994(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2815A>T
AA Mutation p.Asn939Tyr(p.N939Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 30
Mutation Consequence missense_variant
Transcription ID ENST00000264360
Start 133151848:133151848(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1708A>G
AA Mutation p.Asn570Asp(p.N570D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 31
Mutation Consequence missense_variant
Transcription ID ENST00000264360
Start 133152428:133152428(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2288G>A
AA Mutation p.Cys763Tyr(p.C763Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 32
Mutation Consequence missense_variant
Transcription ID ENST00000264360
Start 133150474:133150474(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.334G>A
AA Mutation p.Val112Met(p.V112M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 33
Mutation Consequence missense_variant
Transcription ID ENST00000264360
Start 133151668:133151668(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1528A>G
AA Mutation p.Met510Val(p.M510V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 34
Mutation Consequence missense_variant
Transcription ID ENST00000264360
Start 133150240:133150240(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.100G>A
AA Mutation p.Val34Met(p.V34M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 35
Mutation Consequence missense_variant
Transcription ID ENST00000264360
Start 133150610:133150610(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs754653138
CDS Mutation c.470G>A
AA Mutation p.Arg157His(p.R157H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 36
Mutation Consequence missense_variant
Transcription ID ENST00000264360
Start 133151626:133151626(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1486G>A
AA Mutation p.Ala496Thr(p.A496T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 37
Mutation Consequence missense_variant
Transcription ID ENST00000264360
Start 133150377:133150377(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.237A>G
AA Mutation p.Ile79Met(p.I79M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 38
Mutation Consequence synonymous_variant
Transcription ID ENST00000264360
Start 133151781:133151781(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1641C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 39
Mutation Consequence synonymous_variant
Transcription ID ENST00000264360
Start 133150711:133150711(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.571C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 40
Mutation Consequence synonymous_variant
Transcription ID ENST00000264360
Start 133151850:133151850(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1710C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 41
Mutation Consequence synonymous_variant
Transcription ID ENST00000264360
Start 133150680:133150680(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.540C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 42
Mutation Consequence synonymous_variant
Transcription ID ENST00000264360
Start 133150581:133150581(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs757923593
CDS Mutation c.441C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 43
Mutation Consequence synonymous_variant
Transcription ID ENST00000264360
Start 133152723:133152723(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs111442577
CDS Mutation c.2583C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 44
Mutation Consequence synonymous_variant
Transcription ID ENST00000264360
Start 133151967:133151967(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1827C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 45
Mutation Consequence synonymous_variant
Transcription ID ENST00000264360
Start 133151523:133151523(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1383G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 46
Mutation Consequence synonymous_variant
Transcription ID ENST00000264360
Start 133151079:133151079(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs769286962
CDS Mutation c.939C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 47
Mutation Consequence synonymous_variant
Transcription ID ENST00000264360
Start 133151718:133151718(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs762454585
CDS Mutation c.1578C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 48
Mutation Consequence synonymous_variant
Transcription ID ENST00000264360
Start 133151250:133151250(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1110C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 49
Mutation Consequence synonymous_variant
Transcription ID ENST00000264360
Start 133152627:133152627(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2487C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 50
Mutation Consequence synonymous_variant
Transcription ID ENST00000264360
Start 133154354:133154354(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2679C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 51
Mutation Consequence synonymous_variant
Transcription ID ENST00000264360
Start 133151673:133151673(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1533C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 52
Mutation Consequence synonymous_variant
Transcription ID ENST00000264360
Start 133151295:133151295(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1155C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 53
Mutation Consequence synonymous_variant
Transcription ID ENST00000264360
Start 133163131:133163131(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2952T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 54
Mutation Consequence synonymous_variant
Transcription ID ENST00000264360
Start 133150944:133150944(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs765513404
CDS Mutation c.804C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 55
Mutation Consequence synonymous_variant
Transcription ID ENST00000264360
Start 133152510:133152510(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2370G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 56
Mutation Consequence synonymous_variant
Transcription ID ENST00000264360
Start 133150272:133150272(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.132C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 57
Mutation Consequence synonymous_variant
Transcription ID ENST00000264360
Start 133150800:133150800(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs762772902
CDS Mutation c.660G>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 58
Mutation Consequence synonymous_variant
Transcription ID ENST00000264360
Start 133150239:133150239(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.99C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 59
Mutation Consequence synonymous_variant
Transcription ID ENST00000264360
Start 133151343:133151343(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1203G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 60
Mutation Consequence synonymous_variant
Transcription ID ENST00000264360
Start 133152312:133152312(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2172G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 61
Mutation Consequence synonymous_variant
Transcription ID ENST00000264360
Start 133150287:133150287(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.147G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 62
Mutation Consequence synonymous_variant
Transcription ID ENST00000264360
Start 133151589:133151589(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1449C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 63
Mutation Consequence frameshift_variant
Transcription ID ENST00000264360
Start 133150813:133150813(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.679delC
AA Mutation p.Gln227SerfsTer43(p.Q227Sfs*43)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 64
Mutation Consequence frameshift_variant
Transcription ID ENST00000264360
Start 133151396:133151396(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1261delC
AA Mutation p.Leu421TrpfsTer11(p.L421Wfs*11)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 65
Mutation Consequence frameshift_variant
Transcription ID ENST00000264360
Start 133150494:133150494(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.360delC
AA Mutation p.Ser121LeufsTer7(p.S121Lfs*7)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 66
Mutation Consequence frameshift_variant
Transcription ID ENST00000264360
Start 133151790:133151790(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1654delC
AA Mutation p.Gln552ArgfsTer13(p.Q552Rfs*13)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 67
Mutation Consequence stop_gained
Transcription ID ENST00000264360
Start 133163255:133163255(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3076C>T
AA Mutation p.Arg1026Ter(p.R1026*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript

Rectum Cancer: Gene >> PCDH10

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000264360
Start 133151694:133151694(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1554C>G
AA Mutation p.Ile518Met(p.I518M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000264360
Start 133162977:133162977(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2798G>A
AA Mutation p.Gly933Asp(p.G933D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000264360
Start 133151996:133151996(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1856G>T
AA Mutation p.Ser619Ile(p.S619I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000264360
Start 133150369:133150369(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.229G>A
AA Mutation p.Glu77Lys(p.E77K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000264360
Start 133151569:133151569(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1429G>A
AA Mutation p.Val477Met(p.V477M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000264360
Start 133151160:133151160(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1020G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000264360
Start 133151850:133151850(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1710C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000264360
Start 133151457:133151457(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1317C>T
Mutation Classification Silent
Feature Type Transcript