Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> PTPN13

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000411767
Start 86750479:86750479(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2660C>T
AA Mutation p.Ser887Leu(p.S887L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000411767
Start 86799192:86799192(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6493G>A
AA Mutation p.Asp2165Asn(p.D2165N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000411767
Start 86751041:86751041(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs529404601
CDS Mutation c.3083C>T
AA Mutation p.Ala1028Val(p.A1028V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000411767
Start 86732748:86732748(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1840G>A
AA Mutation p.Ala614Thr(p.A614T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000411767
Start 86750629:86750629(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2810G>T
AA Mutation p.Cys937Phe(p.C937F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000411767
Start 86716550:86716550(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1216A>G
AA Mutation p.Thr406Ala(p.T406A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000411767
Start 86722280:86722280(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1454A>G
AA Mutation p.Glu485Gly(p.E485G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000411767
Start 86750578:86750578(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2759T>A
AA Mutation p.Leu920His(p.L920H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000411767
Start 86750589:86750589(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs763863340
CDS Mutation c.2770C>T
AA Mutation p.Pro924Ser(p.P924S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000411767
Start 86764713:86764713(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4138A>T
AA Mutation p.Ile1380Leu(p.I1380L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000411767
Start 86722270:86722270(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs575836236
CDS Mutation c.1444C>T
AA Mutation p.Arg482Trp(p.R482W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000411767
Start 86775549:86775549(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5788G>A
AA Mutation p.Val1930Ile(p.V1930I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000411767
Start 86701580:86701580(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.974A>G
AA Mutation p.His325Arg(p.H325R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000411767
Start 86814475:86814475(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs746257466
CDS Mutation c.7382A>G
AA Mutation p.Tyr2461Cys(p.Y2461C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000411767
Start 86750877:86750877(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3058A>C
AA Mutation p.Lys1020Gln(p.K1020Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000411767
Start 86758687:86758687(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3323T>G
AA Mutation p.Ile1108Ser(p.I1108S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000411767
Start 86803816:86803816(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6613C>T
AA Mutation p.Arg2205Trp(p.R2205W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000411767
Start 86772810:86772810(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5201C>A
AA Mutation p.Pro1734His(p.P1734H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000411767
Start 86784493:86784493(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs764113622
CDS Mutation c.6053C>T
AA Mutation p.Ser2018Leu(p.S2018L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000411767
Start 86784484:86784484(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6044A>G
AA Mutation p.Asn2015Ser(p.N2015S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000411767
Start 86701426:86701426(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.820C>A
AA Mutation p.Pro274Thr(p.P274T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000411767
Start 86772855:86772855(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs724159902
CDS Mutation c.5246C>T
AA Mutation p.Ser1749Leu(p.S1749L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000411767
Start 86750764:86750764(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs545870212
CDS Mutation c.2945G>A
AA Mutation p.Arg982Gln(p.R982Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000411767
Start 86799121:86799121(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6422A>G
AA Mutation p.Glu2141Gly(p.E2141G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000411767
Start 86803765:86803765(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6562C>T
AA Mutation p.Pro2188Ser(p.P2188S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000411767
Start 86811073:86811073(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7327A>G
AA Mutation p.Met2443Val(p.M2443V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000411767
Start 86803819:86803819(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6616G>T
AA Mutation p.Gly2206Cys(p.G2206C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 28
Mutation Consequence missense_variant
Transcription ID ENST00000411767
Start 86686771:86686771(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.356G>T
AA Mutation p.Ser119Ile(p.S119I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 29
Mutation Consequence synonymous_variant
Transcription ID ENST00000411767
Start 86771449:86771449(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5082T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 30
Mutation Consequence synonymous_variant
Transcription ID ENST00000411767
Start 86809918:86809918(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7233C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 31
Mutation Consequence synonymous_variant
Transcription ID ENST00000411767
Start 86701548:86701548(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.942T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 32
Mutation Consequence synonymous_variant
Transcription ID ENST00000411767
Start 86750855:86750855(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3036A>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 33
Mutation Consequence synonymous_variant
Transcription ID ENST00000411767
Start 86807597:86807597(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6783C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 34
Mutation Consequence synonymous_variant
Transcription ID ENST00000411767
Start 86689169:86689169(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.525G>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 35
Mutation Consequence synonymous_variant
Transcription ID ENST00000411767
Start 86689139:86689139(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.495A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 36
Mutation Consequence synonymous_variant
Transcription ID ENST00000411767
Start 86732648:86732648(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs774699023
CDS Mutation c.1740C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 37
Mutation Consequence synonymous_variant
Transcription ID ENST00000411767
Start 86765415:86765415(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4170C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 38
Mutation Consequence synonymous_variant
Transcription ID ENST00000411767
Start 86785334:86785334(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs754646654
CDS Mutation c.6222C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 39
Mutation Consequence synonymous_variant
Transcription ID ENST00000411767
Start 86751042:86751042(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs771563643
CDS Mutation c.3084G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 40
Mutation Consequence synonymous_variant
Transcription ID ENST00000411767
Start 86701569:86701569(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs776697002
CDS Mutation c.963T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 41
Mutation Consequence synonymous_variant
Transcription ID ENST00000411767
Start 86771296:86771296(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4929C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 42
Mutation Consequence synonymous_variant
Transcription ID ENST00000411767
Start 86803836:86803836(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6633A>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 43
Mutation Consequence synonymous_variant
Transcription ID ENST00000411767
Start 86807645:86807645(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6831C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 44
Mutation Consequence frameshift_variant
Transcription ID ENST00000411767
Start 86769879:86769879(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.4604delA
AA Mutation p.Lys1535SerfsTer16(p.K1535Sfs*16)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 45
Mutation Consequence frameshift_variant
Transcription ID ENST00000411767
Start 86734428:86734428(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1989delT
AA Mutation p.Phe663LeufsTer7(p.F663Lfs*7)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 46
Mutation Consequence frameshift_variant
Transcription ID ENST00000411767
Start 86807799:86807799(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.6988delA
AA Mutation p.Thr2330GlnfsTer13(p.T2330Qfs*13)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 47
Mutation Consequence frameshift_variant
Transcription ID ENST00000411767
Start 86764692:86764692(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.4121delA
AA Mutation p.Asn1374MetfsTer7(p.N1374Mfs*7)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 48
Mutation Consequence stop_gained
Transcription ID ENST00000411767
Start 86693647:86693647(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.607C>T
AA Mutation p.Arg203Ter(p.R203*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 49
Mutation Consequence stop_gained
Transcription ID ENST00000411767
Start 86807826:86807826(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7012C>T
AA Mutation p.Arg2338Ter(p.R2338*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript

Rectum Cancer: Gene >> PTPN13

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000411767
Start 86734827:86734827(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2103G>C
AA Mutation p.Leu701Phe(p.L701F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000411767
Start 86701466:86701466(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.860T>A
AA Mutation p.Ile287Asn(p.I287N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000411767
Start 86771228:86771228(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4861C>T
AA Mutation p.Pro1621Ser(p.P1621S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000411767
Start 86766455:86766455(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4267G>C
AA Mutation p.Gly1423Arg(p.G1423R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000411767
Start 86672430:86672430(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.181T>C
AA Mutation p.Ser61Pro(p.S61P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000411767
Start 86701437:86701437(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.831C>A
AA Mutation p.Phe277Leu(p.F277L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000411767
Start 86745122:86745122(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2644G>T
AA Mutation p.Asp882Tyr(p.D882Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000411767
Start 86750479:86750479(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2660C>T
AA Mutation p.Ser887Leu(p.S887L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000411767
Start 86753056:86753056(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3214A>C
AA Mutation p.Lys1072Gln(p.K1072Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000411767
Start 86762773:86762773(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3600G>T
AA Mutation p.Met1200Ile(p.M1200I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000411767
Start 86762943:86762943(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3770C>A
AA Mutation p.Ser1257Tyr(p.S1257Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000411767
Start 86763049:86763049(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3876G>T
AA Mutation p.Glu1292Asp(p.E1292D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000411767
Start 86767955:86767955(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4468G>T
AA Mutation p.Asp1490Tyr(p.D1490Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000411767
Start 86803840:86803840(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6637C>A
AA Mutation p.Pro2213Thr(p.P2213T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000411767
Start 86809861:86809861(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7176C>G
AA Mutation p.Ile2392Met(p.I2392M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000411767
Start 86635290:86635290(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs770308424
CDS Mutation c.34C>T
AA Mutation p.Arg12Trp(p.R12W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000411767
Start 86734429:86734429(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1985T>G
AA Mutation p.Phe662Cys(p.F662C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence synonymous_variant
Transcription ID ENST00000411767
Start 86750642:86750642(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs748274481
CDS Mutation c.2823G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 19
Mutation Consequence synonymous_variant
Transcription ID ENST00000411767
Start 86807645:86807645(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6831C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 20
Mutation Consequence synonymous_variant
Transcription ID ENST00000411767
Start 86735635:86735635(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2193C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 21
Mutation Consequence synonymous_variant
Transcription ID ENST00000411767
Start 86805291:86805291(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6667T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 22
Mutation Consequence stop_gained
Transcription ID ENST00000411767
Start 86759058:86759058(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3538G>T
AA Mutation p.Glu1180Ter(p.E1180*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence stop_gained
Transcription ID ENST00000411767
Start 86785911:86785911(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6320C>A
AA Mutation p.Ser2107Ter(p.S2107*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence stop_gained
Transcription ID ENST00000411767
Start 86807826:86807826(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7012C>T
AA Mutation p.Arg2338Ter(p.R2338*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript