Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> PTPRD

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000356435
Start 8404588:8404588(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4159G>A
AA Mutation p.Ala1387Thr(p.A1387T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000356435
Start 8404561:8404561(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4186C>T
AA Mutation p.Arg1396Trp(p.R1396W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000356435
Start 8507303:8507303(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1675G>A
AA Mutation p.Glu559Lys(p.E559K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000356435
Start 8484375:8484375(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3157C>A
AA Mutation p.Leu1053Ile(p.L1053I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000356435
Start 8733794:8733794(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.50G>A
AA Mutation p.Arg17His(p.R17H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000356435
Start 8733791:8733791(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs376714429
CDS Mutation c.53C>T
AA Mutation p.Thr18Met(p.T18M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000356435
Start 8636706:8636706(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.203G>T
AA Mutation p.Arg68Ile(p.R68I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000356435
Start 8331661:8331661(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5455G>A
AA Mutation p.Gly1819Arg(p.G1819R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000356435
Start 8504368:8504368(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1715T>C
AA Mutation p.Leu572Pro(p.L572P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000356435
Start 8518097:8518097(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1294A>G
AA Mutation p.Thr432Ala(p.T432A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000356435
Start 8528612:8528612(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.520C>T
AA Mutation p.Arg174Cys(p.R174C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000356435
Start 8499754:8499754(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2215A>C
AA Mutation p.Lys739Gln(p.K739Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000356435
Start 8485810:8485810(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs724159859
CDS Mutation c.3007G>A
AA Mutation p.Gly1003Arg(p.G1003R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000356435
Start 8486143:8486143(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs370631792
CDS Mutation c.2674G>A
AA Mutation p.Val892Ile(p.V892I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000356435
Start 8492931:8492931(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201412075
CDS Mutation c.2398G>A
AA Mutation p.Val800Ile(p.V800I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000356435
Start 8518190:8518190(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1201C>T
AA Mutation p.Arg401Trp(p.R401W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000356435
Start 8521489:8521489(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.749G>A
AA Mutation p.Gly250Asp(p.G250D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000356435
Start 8465518:8465518(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3662G>A
AA Mutation p.Ser1221Asn(p.S1221N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000356435
Start 8485968:8485968(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2849T>G
AA Mutation p.Ile950Ser(p.I950S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000356435
Start 8500899:8500899(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1983G>T
AA Mutation p.Glu661Asp(p.E661D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000356435
Start 8389282:8389282(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4336C>A
AA Mutation p.Gln1446Lys(p.Q1446K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000356435
Start 8501056:8501056(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1826C>T
AA Mutation p.Pro609Leu(p.P609L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000356435
Start 8504274:8504274(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1809A>C
AA Mutation p.Arg603Ser(p.R603S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000356435
Start 8504351:8504351(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1732A>C
AA Mutation p.Asn578His(p.N578H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000356435
Start 8375960:8375960(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4637C>T
AA Mutation p.Ala1546Val(p.A1546V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000356435
Start 8484264:8484264(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3268A>C
AA Mutation p.Asn1090His(p.N1090H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 27
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000356435
Start 8341268:8341268(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4948C>T
AA Mutation p.Arg1650Cys(p.R1650C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 28
Mutation Consequence synonymous_variant
Transcription ID ENST00000356435
Start 8375974:8375974(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4623T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 29
Mutation Consequence synonymous_variant
Transcription ID ENST00000356435
Start 8500812:8500812(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2070T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 30
Mutation Consequence synonymous_variant
Transcription ID ENST00000356435
Start 8465649:8465649(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3531C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 31
Mutation Consequence synonymous_variant
Transcription ID ENST00000356435
Start 8521482:8521482(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs765489687
CDS Mutation c.756C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 32
Mutation Consequence synonymous_variant
Transcription ID ENST00000356435
Start 8341702:8341702(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs753384952
CDS Mutation c.4938C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 33
Mutation Consequence synonymous_variant
Transcription ID ENST00000356435
Start 8500815:8500815(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2067C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 34
Mutation Consequence synonymous_variant
Transcription ID ENST00000356435
Start 8341948:8341948(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs138863975
CDS Mutation c.4692C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 35
Mutation Consequence synonymous_variant
Transcription ID ENST00000356435
Start 8528682:8528682(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.450T>C
Mutation Classification Silent
Feature Type Transcript

Rectum Cancer: Gene >> PTPRD

Mutation ID 1
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000356435
Start 8471084:8471084(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3415G>T
AA Mutation p.Gly1139Cys(p.G1139C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000356435
Start 8389254:8389254(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4364C>G
AA Mutation p.Thr1455Arg(p.T1455R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000356435
Start 8484163:8484163(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs781290016
CDS Mutation c.3369G>A
AA Mutation p.Met1123Ile(p.M1123I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000356435
Start 8404560:8404560(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs781289256
CDS Mutation c.4187G>A
AA Mutation p.Arg1396Gln(p.R1396Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000356435
Start 8484375:8484375(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3157C>A
AA Mutation p.Leu1053Ile(p.L1053I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000356435
Start 8518036:8518036(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1355G>T
AA Mutation p.Arg452Ile(p.R452I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000356435
Start 8484226:8484226(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3306G>T
AA Mutation p.Lys1102Asn(p.K1102N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000356435
Start 8500788:8500788(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2094G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 9
Mutation Consequence stop_gained
Transcription ID ENST00000356435
Start 8518286:8518286(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1105G>T
AA Mutation p.Glu369Ter(p.E369*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript