Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> TNR

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000263525
Start 175391320:175391320(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1475G>A
AA Mutation p.Arg492His(p.R492H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000263525
Start 175324400:175324400(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs778628919
CDS Mutation c.3913C>T
AA Mutation p.Arg1305Trp(p.R1305W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000263525
Start 175366042:175366042(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs551588483
CDS Mutation c.2150G>A
AA Mutation p.Arg717Gln(p.R717Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000263525
Start 175363746:175363746(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2669C>A
AA Mutation p.Ser890Tyr(p.S890Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000263525
Start 175367221:175367221(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2040G>T
AA Mutation p.Met680Ile(p.M680I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000263525
Start 175365932:175365932(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs370853708
CDS Mutation c.2260G>A
AA Mutation p.Val754Ile(p.V754I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000263525
Start 175324493:175324493(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs570797805
CDS Mutation c.3820C>T
AA Mutation p.Arg1274Cys(p.R1274C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000263525
Start 175403415:175403415(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201187422
CDS Mutation c.701G>A
AA Mutation p.Arg234Gln(p.R234Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000263525
Start 175403422:175403422(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.694G>A
AA Mutation p.Glu232Lys(p.E232K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000263525
Start 175406329:175406329(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.386G>C
AA Mutation p.Ser129Thr(p.S129T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000263525
Start 175379660:175379660(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1855G>A
AA Mutation p.Ala619Thr(p.A619T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000263525
Start 175355607:175355607(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3145G>A
AA Mutation p.Ala1049Thr(p.A1049T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000263525
Start 175406297:175406297(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.418C>T
AA Mutation p.Arg140Trp(p.R140W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000263525
Start 175403314:175403314(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.802G>A
AA Mutation p.Gly268Arg(p.G268R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000263525
Start 175335786:175335786(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3556G>A
AA Mutation p.Gly1186Ser(p.G1186S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000263525
Start 175386085:175386085(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1724G>C
AA Mutation p.Ser575Thr(p.S575T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000263525
Start 175396603:175396603(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1181G>A
AA Mutation p.Ser394Asn(p.S394N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000263525
Start 175406258:175406258(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.457G>T
AA Mutation p.Asp153Tyr(p.D153Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000263525
Start 175403297:175403297(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.819G>T
AA Mutation p.Lys273Asn(p.K273N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000263525
Start 175365273:175365273(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs141636585
CDS Mutation c.2324G>A
AA Mutation p.Arg775His(p.R775H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000263525
Start 175363810:175363810(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2605G>C
AA Mutation p.Asp869His(p.D869H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000263525
Start 175396693:175396693(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1091T>C
AA Mutation p.Leu364Pro(p.L364P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000263525
Start 175403505:175403505(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.611G>T
AA Mutation p.Cys204Phe(p.C204F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000263525
Start 175406420:175406420(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.295G>A
AA Mutation p.Ala99Thr(p.A99T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000263525
Start 175323421:175323421(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4013T>G
AA Mutation p.Met1338Arg(p.M1338R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000263525
Start 175356389:175356389(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3048C>A
AA Mutation p.His1016Gln(p.H1016Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000263525
Start 175323413:175323413(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4021C>T
AA Mutation p.Arg1341Cys(p.R1341C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 28
Mutation Consequence missense_variant
Transcription ID ENST00000263525
Start 175366012:175366012(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2180C>T
AA Mutation p.Ala727Val(p.A727V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 29
Mutation Consequence missense_variant
Transcription ID ENST00000263525
Start 175363785:175363785(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2630A>C
AA Mutation p.Lys877Thr(p.K877T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 30
Mutation Consequence missense_variant
Transcription ID ENST00000263525
Start 175356418:175356418(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs774052903
CDS Mutation c.3019C>T
AA Mutation p.Arg1007Trp(p.R1007W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 31
Mutation Consequence missense_variant
Transcription ID ENST00000263525
Start 175330152:175330152(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs755878985
CDS Mutation c.3715G>A
AA Mutation p.Ala1239Thr(p.A1239T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 32
Mutation Consequence missense_variant
Transcription ID ENST00000263525
Start 175365913:175365913(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2279G>A
AA Mutation p.Arg760Gln(p.R760Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 33
Mutation Consequence missense_variant
Transcription ID ENST00000263525
Start 175362707:175362707(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773416045
CDS Mutation c.2810G>A
AA Mutation p.Arg937Gln(p.R937Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 34
Mutation Consequence missense_variant
Transcription ID ENST00000263525
Start 175386158:175386158(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200243334
CDS Mutation c.1651C>T
AA Mutation p.Arg551Trp(p.R551W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 35
Mutation Consequence missense_variant
Transcription ID ENST00000263525
Start 175403517:175403517(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.599C>T
AA Mutation p.Ser200Leu(p.S200L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 36
Mutation Consequence missense_variant
Transcription ID ENST00000263525
Start 175393862:175393862(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201687672
CDS Mutation c.1274C>T
AA Mutation p.Thr425Met(p.T425M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 37
Mutation Consequence synonymous_variant
Transcription ID ENST00000263525
Start 175386099:175386099(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs746969510
CDS Mutation c.1710C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 38
Mutation Consequence synonymous_variant
Transcription ID ENST00000263525
Start 175365182:175365182(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2415T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 39
Mutation Consequence synonymous_variant
Transcription ID ENST00000263525
Start 175396743:175396743(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs772070027
CDS Mutation c.1041C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 40
Mutation Consequence synonymous_variant
Transcription ID ENST00000263525
Start 175403438:175403438(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.678C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 41
Mutation Consequence synonymous_variant
Transcription ID ENST00000263525
Start 175359724:175359724(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2862C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 42
Mutation Consequence synonymous_variant
Transcription ID ENST00000263525
Start 175330102:175330102(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3765C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 43
Mutation Consequence synonymous_variant
Transcription ID ENST00000263525
Start 175330120:175330120(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs149559732
CDS Mutation c.3747C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 44
Mutation Consequence synonymous_variant
Transcription ID ENST00000263525
Start 175330159:175330159(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs755070959
CDS Mutation c.3708C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 45
Mutation Consequence synonymous_variant
Transcription ID ENST00000263525
Start 175406514:175406514(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs755838255
CDS Mutation c.201C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 46
Mutation Consequence synonymous_variant
Transcription ID ENST00000263525
Start 175362730:175362730(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs772789738
CDS Mutation c.2787C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 47
Mutation Consequence synonymous_variant
Transcription ID ENST00000263525
Start 175365933:175365933(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs549333643
CDS Mutation c.2259C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 48
Mutation Consequence synonymous_variant
Transcription ID ENST00000263525
Start 175396713:175396713(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1071C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 49
Mutation Consequence synonymous_variant
Transcription ID ENST00000263525
Start 175386216:175386216(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs375626142
CDS Mutation c.1593C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 50
Mutation Consequence stop_gained
Transcription ID ENST00000263525
Start 175363732:175363732(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2683C>T
AA Mutation p.Arg895Ter(p.R895*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 51
Mutation Consequence stop_gained
Transcription ID ENST00000263525
Start 175363763:175363763(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs758352909
CDS Mutation c.2652G>A
AA Mutation p.Trp884Ter(p.W884*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 52
Mutation Consequence stop_gained
Transcription ID ENST00000263525
Start 175365082:175365082(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2515G>T
AA Mutation p.Glu839Ter(p.E839*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 53
Mutation Consequence stop_gained
Transcription ID ENST00000263525
Start 175406261:175406261(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.454C>T
AA Mutation p.Arg152Ter(p.R152*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 54
Mutation Consequence frameshift_variant
Transcription ID ENST00000263525
Start 175403479:175403480(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.636_637insT
AA Mutation p.Val213CysfsTer10(p.V213Cfs*10)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript

Rectum Cancer: Gene >> TNR

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000263525
Start 175391395:175391395(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs753755790
CDS Mutation c.1400C>T
AA Mutation p.Thr467Met(p.T467M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000263525
Start 175356418:175356418(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs774052903
CDS Mutation c.3019C>T
AA Mutation p.Arg1007Trp(p.R1007W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000263525
Start 175396658:175396658(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1126G>T
AA Mutation p.Asp376Tyr(p.D376Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000263525
Start 175403416:175403416(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs371035988
CDS Mutation c.700C>T
AA Mutation p.Arg234Trp(p.R234W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000263525
Start 175403341:175403341(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs775102963
CDS Mutation c.775G>A
AA Mutation p.Glu259Lys(p.E259K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000263525
Start 175359719:175359719(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2867C>A
AA Mutation p.Pro956His(p.P956H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000263525
Start 175365019:175365019(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2578A>T
AA Mutation p.Ile860Phe(p.I860F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000263525
Start 175396738:175396738(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1046C>T
AA Mutation p.Pro349Leu(p.P349L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000263525
Start 175406246:175406246(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.469G>A
AA Mutation p.Ala157Thr(p.A157T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000263525
Start 175363742:175363742(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs760178073
CDS Mutation c.2673C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000263525
Start 175393861:175393861(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs781713010
CDS Mutation c.1275G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000263525
Start 175354413:175354413(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3360C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000263525
Start 175386099:175386099(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs746969510
CDS Mutation c.1710C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 14
Mutation Consequence synonymous_variant
Transcription ID ENST00000263525
Start 175386087:175386087(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs757250730
CDS Mutation c.1722C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 15
Mutation Consequence synonymous_variant
Transcription ID ENST00000263525
Start 175330129:175330129(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs377731803
CDS Mutation c.3738C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 16
Mutation Consequence synonymous_variant
Transcription ID ENST00000263525
Start 175362730:175362730(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs772789738
CDS Mutation c.2787C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 17
Mutation Consequence synonymous_variant
Transcription ID ENST00000263525
Start 175386216:175386216(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs375626142
CDS Mutation c.1593C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 18
Mutation Consequence synonymous_variant
Transcription ID ENST00000263525
Start 175406292:175406292(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.423C>T
Mutation Classification Silent
Feature Type Transcript