Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CDH10

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000264463
Start 24505186:24505186(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1319C>A
AA Mutation p.Ser440Tyr(p.S440Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000264463
Start 24509777:24509777(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs138533676
CDS Mutation c.1045G>A
AA Mutation p.Glu349Lys(p.E349K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000264463
Start 24593473:24593473(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.18T>A
AA Mutation p.Phe6Leu(p.F6L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000264463
Start 24509794:24509794(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1028T>A
AA Mutation p.Leu343His(p.L343H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000264463
Start 24487970:24487970(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2060G>A
AA Mutation p.Arg687Gln(p.R687Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000264463
Start 24505235:24505235(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1270C>T
AA Mutation p.Arg424Cys(p.R424C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000264463
Start 24487743:24487743(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2287G>A
AA Mutation p.Asp763Asn(p.D763N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000264463
Start 24509584:24509584(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1238C>A
AA Mutation p.Ser413Tyr(p.S413Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000264463
Start 24537659:24537659(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.247G>T
AA Mutation p.Asp83Tyr(p.D83Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000264463
Start 24593292:24593292(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.199T>C
AA Mutation p.Tyr67His(p.Y67H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000264463
Start 24487965:24487965(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2065G>T
AA Mutation p.Asp689Tyr(p.D689Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000264463
Start 24487686:24487686(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2344G>C
AA Mutation p.Gly782Arg(p.G782R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000264463
Start 24491742:24491742(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1710C>A
AA Mutation p.Asp570Glu(p.D570E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000264463
Start 24491819:24491819(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1633G>A
AA Mutation p.Ala545Thr(p.A545T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000264463
Start 24505144:24505144(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1361G>T
AA Mutation p.Trp454Leu(p.W454L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000264463
Start 24498457:24498457(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1456G>T
AA Mutation p.Ala486Ser(p.A486S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000264463
Start 24511499:24511499(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs149518689
CDS Mutation c.830G>A
AA Mutation p.Arg277Gln(p.R277Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000264463
Start 24487949:24487949(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs543550761
CDS Mutation c.2081C>T
AA Mutation p.Thr694Met(p.T694M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000264463
Start 24487829:24487829(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2201C>T
AA Mutation p.Ala734Val(p.A734V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000264463
Start 24537523:24537523(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs369925572
CDS Mutation c.383G>A
AA Mutation p.Arg128His(p.R128H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000264463
Start 24487862:24487862(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs763423183
CDS Mutation c.2168T>C
AA Mutation p.Leu723Pro(p.L723P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000264463
Start 24487898:24487898(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2132G>A
AA Mutation p.Arg711Gln(p.R711Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000264463
Start 24492863:24492863(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1578C>A
AA Mutation p.Phe526Leu(p.F526L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000264463
Start 24487879:24487879(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs751881000
CDS Mutation c.2151G>T
AA Mutation p.Arg717Ser(p.R717S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000264463
Start 24491803:24491803(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1649G>T
AA Mutation p.Arg550Ile(p.R550I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000264463
Start 24492873:24492873(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1568A>C
AA Mutation p.Lys523Thr(p.K523T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000264463
Start 24593268:24593268(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs770889275
CDS Mutation c.223G>A
AA Mutation p.Val75Ile(p.V75I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 28
Mutation Consequence missense_variant
Transcription ID ENST00000264463
Start 24487863:24487863(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2167C>T
AA Mutation p.Leu723Phe(p.L723F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 29
Mutation Consequence missense_variant
Transcription ID ENST00000264463
Start 24498475:24498475(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1438T>G
AA Mutation p.Leu480Val(p.L480V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 30
Mutation Consequence missense_variant
Transcription ID ENST00000264463
Start 24487937:24487937(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2093C>A
AA Mutation p.Pro698His(p.P698H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 31
Mutation Consequence missense_variant
Transcription ID ENST00000264463
Start 24505225:24505225(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1280A>G
AA Mutation p.Asp427Gly(p.D427G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 32
Mutation Consequence missense_variant
Transcription ID ENST00000264463
Start 24492868:24492868(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1573T>G
AA Mutation p.Phe525Val(p.F525V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 33
Mutation Consequence missense_variant
Transcription ID ENST00000264463
Start 24511428:24511428(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.901A>C
AA Mutation p.Asn301His(p.N301H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 34
Mutation Consequence missense_variant
Transcription ID ENST00000264463
Start 24593302:24593302(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.189A>T
AA Mutation p.Leu63Phe(p.L63F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 35
Mutation Consequence missense_variant
Transcription ID ENST00000264463
Start 24488150:24488150(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1880T>C
AA Mutation p.Ile627Thr(p.I627T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 36
Mutation Consequence synonymous_variant
Transcription ID ENST00000264463
Start 24487924:24487924(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs753973333
CDS Mutation c.2106T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 37
Mutation Consequence synonymous_variant
Transcription ID ENST00000264463
Start 24509814:24509814(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1008C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 38
Mutation Consequence synonymous_variant
Transcription ID ENST00000264463
Start 24511410:24511410(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.919C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 39
Mutation Consequence synonymous_variant
Transcription ID ENST00000264463
Start 24498497:24498497(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs139927244
CDS Mutation c.1416C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 40
Mutation Consequence synonymous_variant
Transcription ID ENST00000264463
Start 24509802:24509802(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1020C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 41
Mutation Consequence synonymous_variant
Transcription ID ENST00000264463
Start 24488137:24488137(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1893T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 42
Mutation Consequence synonymous_variant
Transcription ID ENST00000264463
Start 24593449:24593449(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs766989977
CDS Mutation c.42A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 43
Mutation Consequence frameshift_variant
Transcription ID ENST00000264463
Start 24487724:24487724(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2306delG
AA Mutation p.Gly769AlafsTer7(p.G769Afs*7)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 44
Mutation Consequence frameshift_variant
Transcription ID ENST00000264463
Start 24488110:24488110(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1920delA
AA Mutation p.Glu641SerfsTer3(p.E641Sfs*3)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 45
Mutation Consequence frameshift_variant
Transcription ID ENST00000264463
Start 24492864:24492864(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1577delT
AA Mutation p.Phe526SerfsTer3(p.F526Sfs*3)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 46
Mutation Consequence frameshift_variant
Transcription ID ENST00000264463
Start 24537600:24537600(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.306delT
AA Mutation p.Phe102LeufsTer36(p.F102Lfs*36)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 47
Mutation Consequence frameshift_variant
Transcription ID ENST00000264463
Start 24537584:24537584(version: GRCh38)
Mutation Type DEL
dbSNP_RS rs748395403
CDS Mutation c.322delA
AA Mutation p.Thr108GlnfsTer30(p.T108Qfs*30)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 48
Mutation Consequence frameshift_variant
Transcription ID ENST00000264463
Start 24535115:24535115(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.811delC
AA Mutation p.Gln271ArgfsTer34(p.Q271Rfs*34)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 49
Mutation Consequence stop_gained
Transcription ID ENST00000264463
Start 24487781:24487781(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2249C>A
AA Mutation p.Ser750Ter(p.S750*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 50
Mutation Consequence frameshift_variant
Transcription ID ENST00000264463
Start 24492863:24492864(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.1577dupT
AA Mutation p.Ser527GlnfsTer14(p.S527Qfs*14)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 51
Mutation Consequence frameshift_variant
Transcription ID ENST00000264463
Start 24487975:24487976(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.2054dupA
AA Mutation p.Leu686AlafsTer22(p.L686Afs*22)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 52
Mutation Consequence frameshift_variant
Transcription ID ENST00000264463
Start 24537583:24537584(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.322dupA
AA Mutation p.Thr108AsnfsTer3(p.T108Nfs*3)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 53
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000264463
Start 24537676:24537676(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.232-2A>T
Mutation Classification Splice_Site
Feature Type Transcript

Rectum Cancer: Gene >> CDH10

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000264463
Start 24487965:24487965(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2065G>A
AA Mutation p.Asp689Asn(p.D689N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000264463
Start 24492920:24492920(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1521A>G
AA Mutation p.Ile507Met(p.I507M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000264463
Start 24509813:24509813(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1009G>A
AA Mutation p.Asp337Asn(p.D337N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000264463
Start 24498487:24498487(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1426T>C
AA Mutation p.Phe476Leu(p.F476L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000264463
Start 24511385:24511385(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.944A>G
AA Mutation p.Asp315Gly(p.D315G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000264463
Start 24593473:24593473(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.18T>G
AA Mutation p.Phe6Leu(p.F6L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000264463
Start 24537522:24537522(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768905224
CDS Mutation c.384C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000264463
Start 24593311:24593311(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.180A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 9
Mutation Consequence stop_gained
Transcription ID ENST00000264463
Start 24487701:24487701(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2329G>T
AA Mutation p.Glu777Ter(p.E777*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript