Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CDHR2

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000261944
Start 176576150:176576150(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1159G>A
AA Mutation p.Asp387Asn(p.D387N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000261944
Start 176577438:176577438(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs749182757
CDS Mutation c.1234G>A
AA Mutation p.Asp412Asn(p.D412N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000261944
Start 176589386:176589386(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3065C>T
AA Mutation p.Ala1022Val(p.A1022V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000261944
Start 176577647:176577647(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs762901848
CDS Mutation c.1361C>T
AA Mutation p.Thr454Ile(p.T454I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000261944
Start 176590145:176590145(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3274C>T
AA Mutation p.Arg1092Trp(p.R1092W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000261944
Start 176591218:176591218(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs751180171
CDS Mutation c.3548G>A
AA Mutation p.Arg1183Gln(p.R1183Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000261944
Start 176589346:176589346(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773697758
CDS Mutation c.3025G>A
AA Mutation p.Asp1009Asn(p.D1009N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000261944
Start 176584613:176584613(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2332G>A
AA Mutation p.Val778Met(p.V778M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000261944
Start 176577424:176577424(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1220C>T
AA Mutation p.Ser407Leu(p.S407L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000261944
Start 176586823:176586823(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs139666636
CDS Mutation c.2837G>A
AA Mutation p.Arg946Gln(p.R946Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000261944
Start 176595598:176595598(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs373675182
CDS Mutation c.3859C>T
AA Mutation p.Arg1287Trp(p.R1287W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000261944
Start 176591418:176591418(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3668T>C
AA Mutation p.Leu1223Pro(p.L1223P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000261944
Start 176589553:176589553(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3143G>T
AA Mutation p.Arg1048Leu(p.R1048L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence synonymous_variant
Transcription ID ENST00000261944
Start 176577548:176577548(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs149193999
CDS Mutation c.1344G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 15
Mutation Consequence synonymous_variant
Transcription ID ENST00000261944
Start 176584588:176584588(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2307G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 16
Mutation Consequence synonymous_variant
Transcription ID ENST00000261944
Start 176577515:176577515(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs749764857
CDS Mutation c.1311G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 17
Mutation Consequence synonymous_variant
Transcription ID ENST00000261944
Start 176590274:176590274(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs371974737
CDS Mutation c.3297C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 18
Mutation Consequence synonymous_variant
Transcription ID ENST00000261944
Start 176581366:176581366(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1842C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 19
Mutation Consequence synonymous_variant
Transcription ID ENST00000261944
Start 176575752:176575752(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768189176
CDS Mutation c.873C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 20
Mutation Consequence synonymous_variant
Transcription ID ENST00000261944
Start 176591455:176591455(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3705C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 21
Mutation Consequence frameshift_variant
Transcription ID ENST00000261944
Start 176584639:176584639(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2363delG
AA Mutation p.Gly788ValfsTer4(p.G788Vfs*4)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 22
Mutation Consequence frameshift_variant
Transcription ID ENST00000261944
Start 176576133:176576133(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1147delC
AA Mutation p.Arg383AlafsTer51(p.R383Afs*51)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 23
Mutation Consequence frameshift_variant
Transcription ID ENST00000261944
Start 176574097:176574098(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.420_421insTGTAGAG
AA Mutation p.Ser141CysfsTer13(p.S141Cfs*13)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 24
Mutation Consequence frameshift_variant
Transcription ID ENST00000261944
Start 176574138:176574139(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.461_462insAT
AA Mutation p.Ser155CysfsTer10(p.S155Cfs*10)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript

Rectum Cancer: Gene >> CDHR2

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000261944
Start 176578457:176578457(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1667T>A
AA Mutation p.Leu556Gln(p.L556Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000261944
Start 176584452:176584452(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs113163991
CDS Mutation c.2171C>T
AA Mutation p.Thr724Met(p.T724M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000261944
Start 176584566:176584566(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs749597145
CDS Mutation c.2285C>T
AA Mutation p.Pro762Leu(p.P762L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000261944
Start 176575349:176575349(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs762273064
CDS Mutation c.691G>A
AA Mutation p.Val231Met(p.V231M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000261944
Start 176575971:176575971(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.980A>G
AA Mutation p.Asn327Ser(p.N327S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000261944
Start 176571257:176571257(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs772065485
CDS Mutation c.360C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000261944
Start 176568736:176568736(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.183G>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 8
Mutation Consequence stop_gained
Transcription ID ENST00000261944
Start 176589082:176589082(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2908C>T
AA Mutation p.Arg970Ter(p.R970*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript