Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> PTPRS

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000357368
Start 5221214:5221214(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3241A>G
AA Mutation p.Thr1081Ala(p.T1081A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000357368
Start 5244437:5244437(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1034C>T
AA Mutation p.Ala345Val(p.A345V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000357368
Start 5210564:5210564(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5392C>T
AA Mutation p.Arg1798Cys(p.R1798C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000357368
Start 5212044:5212044(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs749770933
CDS Mutation c.4976G>A
AA Mutation p.Arg1659His(p.R1659H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000357368
Start 5273582:5273582(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs146675930
CDS Mutation c.239C>T
AA Mutation p.Thr80Met(p.T80M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000357368
Start 5218793:5218793(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773998457
CDS Mutation c.3929C>T
AA Mutation p.Pro1310Leu(p.P1310L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000357368
Start 5274299:5274299(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.137C>T
AA Mutation p.Ser46Leu(p.S46L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000357368
Start 5244179:5244179(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs760369713
CDS Mutation c.1292G>A
AA Mutation p.Arg431Gln(p.R431Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000357368
Start 5211722:5211722(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs148218543
CDS Mutation c.5102A>G
AA Mutation p.Asn1701Ser(p.N1701S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000357368
Start 5214685:5214685(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs369756620
CDS Mutation c.4370G>A
AA Mutation p.Cys1457Tyr(p.C1457Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000357368
Start 5238984:5238984(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1784C>T
AA Mutation p.Ala595Val(p.A595V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000357368
Start 5212450:5212450(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4656T>A
AA Mutation p.Phe1552Leu(p.F1552L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000357368
Start 5244197:5244197(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1274C>A
AA Mutation p.Ala425Asp(p.A425D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000357368
Start 5208004:5208004(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs752031088
CDS Mutation c.5696G>A
AA Mutation p.Arg1899Gln(p.R1899Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000357368
Start 5221073:5221073(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs371881792
CDS Mutation c.3382G>A
AA Mutation p.Val1128Ile(p.V1128I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000357368
Start 5212359:5212359(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs777981018
CDS Mutation c.4747G>A
AA Mutation p.Gly1583Ser(p.G1583S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000357368
Start 5208050:5208050(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs759155627
CDS Mutation c.5650G>A
AA Mutation p.Val1884Met(p.V1884M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000357368
Start 5240203:5240203(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1700G>T
AA Mutation p.Arg567Leu(p.R567L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000357368
Start 5215547:5215547(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs558948003
CDS Mutation c.4145C>T
AA Mutation p.Thr1382Met(p.T1382M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000357368
Start 5244138:5244138(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1333G>A
AA Mutation p.Val445Met(p.V445M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000357368
Start 5210785:5210785(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs758652323
CDS Mutation c.5255C>T
AA Mutation p.Ala1752Val(p.A1752V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000357368
Start 5244057:5244057(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747170106
CDS Mutation c.1414G>A
AA Mutation p.Val472Met(p.V472M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000357368
Start 5245965:5245965(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.799G>A
AA Mutation p.Val267Met(p.V267M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000357368
Start 5244186:5244186(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs754224013
CDS Mutation c.1285G>A
AA Mutation p.Ala429Thr(p.A429T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000357368
Start 5215566:5215566(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200850387
CDS Mutation c.4126G>A
AA Mutation p.Ala1376Thr(p.A1376T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000357368
Start 5240257:5240257(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs750655279
CDS Mutation c.1646G>A
AA Mutation p.Arg549Gln(p.R549Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000357368
Start 5214581:5214581(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs369295620
CDS Mutation c.4474C>T
AA Mutation p.Arg1492Trp(p.R1492W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 28
Mutation Consequence missense_variant
Transcription ID ENST00000357368
Start 5220087:5220087(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs142918634
CDS Mutation c.3617G>A
AA Mutation p.Arg1206Gln(p.R1206Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 29
Mutation Consequence missense_variant
Transcription ID ENST00000357368
Start 5211663:5211663(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5161C>T
AA Mutation p.Arg1721Trp(p.R1721W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 30
Mutation Consequence missense_variant
Transcription ID ENST00000357368
Start 5258053:5258053(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs759053243
CDS Mutation c.670G>A
AA Mutation p.Val224Met(p.V224M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 31
Mutation Consequence missense_variant
Transcription ID ENST00000357368
Start 5238991:5238991(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs775100072
CDS Mutation c.1777C>T
AA Mutation p.Arg593Cys(p.R593C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 32
Mutation Consequence missense_variant
Transcription ID ENST00000357368
Start 5243964:5243964(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1507G>A
AA Mutation p.Ala503Thr(p.A503T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 33
Mutation Consequence missense_variant
Transcription ID ENST00000357368
Start 5231316:5231316(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2149G>A
AA Mutation p.Glu717Lys(p.E717K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 34
Mutation Consequence missense_variant
Transcription ID ENST00000357368
Start 5231486:5231486(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200771602
CDS Mutation c.1979C>T
AA Mutation p.Pro660Leu(p.P660L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 35
Mutation Consequence missense_variant
Transcription ID ENST00000357368
Start 5244107:5244107(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1364G>A
AA Mutation p.Gly455Asp(p.G455D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 36
Mutation Consequence missense_variant
Transcription ID ENST00000357368
Start 5231567:5231567(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1898C>T
AA Mutation p.Thr633Met(p.T633M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 37
Mutation Consequence missense_variant
Transcription ID ENST00000357368
Start 5208040:5208040(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5660C>T
AA Mutation p.Thr1887Met(p.T1887M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 38
Mutation Consequence missense_variant
Transcription ID ENST00000357368
Start 5218509:5218509(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3959G>A
AA Mutation p.Arg1320His(p.R1320H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 39
Mutation Consequence missense_variant
Transcription ID ENST00000357368
Start 5218440:5218440(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201934952
CDS Mutation c.4028G>A
AA Mutation p.Arg1343His(p.R1343H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 40
Mutation Consequence missense_variant
Transcription ID ENST00000357368
Start 5244381:5244381(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs377318412
CDS Mutation c.1090G>A
AA Mutation p.Val364Ile(p.V364I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 41
Mutation Consequence synonymous_variant
Transcription ID ENST00000357368
Start 5225773:5225773(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2448C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 42
Mutation Consequence synonymous_variant
Transcription ID ENST00000357368
Start 5212169:5212169(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4851C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 43
Mutation Consequence synonymous_variant
Transcription ID ENST00000357368
Start 5231443:5231443(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2022C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 44
Mutation Consequence synonymous_variant
Transcription ID ENST00000357368
Start 5214385:5214385(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs780451788
CDS Mutation c.4590C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 45
Mutation Consequence synonymous_variant
Transcription ID ENST00000357368
Start 5214654:5214654(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs144710133
CDS Mutation c.4401G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 46
Mutation Consequence synonymous_variant
Transcription ID ENST00000357368
Start 5244376:5244376(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs149022837
CDS Mutation c.1095C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 47
Mutation Consequence synonymous_variant
Transcription ID ENST00000357368
Start 5215528:5215528(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs140530332
CDS Mutation c.4164C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 48
Mutation Consequence synonymous_variant
Transcription ID ENST00000357368
Start 5223164:5223164(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2628G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 49
Mutation Consequence synonymous_variant
Transcription ID ENST00000357368
Start 5265099:5265099(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201540749
CDS Mutation c.477C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 50
Mutation Consequence synonymous_variant
Transcription ID ENST00000357368
Start 5229575:5229575(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2265C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 51
Mutation Consequence synonymous_variant
Transcription ID ENST00000357368
Start 5238971:5238971(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200933180
CDS Mutation c.1797G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 52
Mutation Consequence synonymous_variant
Transcription ID ENST00000357368
Start 5245831:5245831(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201711435
CDS Mutation c.933C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 53
Mutation Consequence synonymous_variant
Transcription ID ENST00000357368
Start 5238998:5238998(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1770C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 54
Mutation Consequence synonymous_variant
Transcription ID ENST00000357368
Start 5210757:5210757(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201047108
CDS Mutation c.5283G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 55
Mutation Consequence synonymous_variant
Transcription ID ENST00000357368
Start 5238947:5238947(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs763617364
CDS Mutation c.1821C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 56
Mutation Consequence synonymous_variant
Transcription ID ENST00000357368
Start 5212214:5212214(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs115634987
CDS Mutation c.4806C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 57
Mutation Consequence frameshift_variant
Transcription ID ENST00000357368
Start 5231438:5231438(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2027delC
AA Mutation p.Pro676ArgfsTer134(p.P676Rfs*134)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 58
Mutation Consequence frameshift_variant
Transcription ID ENST00000357368
Start 5244238:5244238(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1233delG
AA Mutation p.Ser414AlafsTer30(p.S414Afs*30)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 59
Mutation Consequence frameshift_variant
Transcription ID ENST00000357368
Start 5244232:5244232(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1239delC
AA Mutation p.Ser414AlafsTer30(p.S414Afs*30)
Mutation Classification Frame_Shift_Del
Feature Type Transcript

Rectum Cancer: Gene >> PTPRS

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000357368
Start 5244258:5244258(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1213G>A
AA Mutation p.Val405Ile(p.V405I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence synonymous_variant
Transcription ID ENST00000357368
Start 5212393:5212393(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4713G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 3
Mutation Consequence splice_donor_variant
Transcription ID ENST00000357368
Start 5218418:5218418(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4048+2T>C
Mutation Classification Splice_Site
Feature Type Transcript