Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ALK

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000389048
Start 29196804:29196804(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4130C>A
AA Mutation p.Ala1377Asp(p.A1377D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000389048
Start 29920041:29920041(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.619G>C
AA Mutation p.Ala207Pro(p.A207P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000389048
Start 29193651:29193651(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4436C>T
AA Mutation p.Ala1479Val(p.A1479V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000389048
Start 29383752:29383752(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1262C>T
AA Mutation p.Ala421Val(p.A421V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000389048
Start 29920086:29920086(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs770006984
CDS Mutation c.574G>A
AA Mutation p.Glu192Lys(p.E192K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000389048
Start 29222605:29222605(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs55760835
CDS Mutation c.3362G>A
AA Mutation p.Gly1121Asp(p.G1121D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000389048
Start 29920146:29920146(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.514G>A
AA Mutation p.Glu172Lys(p.E172K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000389048
Start 29318304:29318304(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1647G>T
AA Mutation p.Glu549Asp(p.E549D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000389048
Start 29196835:29196835(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4099C>A
AA Mutation p.Gln1367Lys(p.Q1367K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000389048
Start 29275123:29275123(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2017C>A
AA Mutation p.Gln673Lys(p.Q673K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000389048
Start 29239777:29239777(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs187200776
CDS Mutation c.2258G>A
AA Mutation p.Arg753Gln(p.R753Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000389048
Start 29196843:29196843(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4091A>C
AA Mutation p.Gln1364Pro(p.Q1364P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000389048
Start 29232361:29232361(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2575G>C
AA Mutation p.Glu859Gln(p.E859Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000389048
Start 29193781:29193781(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201129468
CDS Mutation c.4306C>T
AA Mutation p.Arg1436Cys(p.R1436C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000389048
Start 29233639:29233639(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2413A>G
AA Mutation p.Ile805Val(p.I805V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000389048
Start 29694928:29694928(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201750304
CDS Mutation c.874C>T
AA Mutation p.Arg292Cys(p.R292C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000389048
Start 29532105:29532105(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.964C>A
AA Mutation p.Leu322Ile(p.L322I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000389048
Start 29328457:29328457(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1307C>T
AA Mutation p.Ala436Val(p.A436V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000389048
Start 29220725:29220725(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747643140
CDS Mutation c.3626G>A
AA Mutation p.Arg1209Gln(p.R1209Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000389048
Start 29383834:29383834(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs775514690
CDS Mutation c.1180G>A
AA Mutation p.Gly394Arg(p.G394R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000389048
Start 29233629:29233629(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2423A>G
AA Mutation p.Asn808Ser(p.N808S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000389048
Start 29920034:29920034(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.626G>A
AA Mutation p.Arg209His(p.R209H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000389048
Start 29318335:29318335(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1616T>G
AA Mutation p.Phe539Cys(p.F539C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000389048
Start 29694931:29694931(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs748854412
CDS Mutation c.871C>T
AA Mutation p.Arg291Cys(p.R291C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000389048
Start 29920098:29920098(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.562C>T
AA Mutation p.Arg188Cys(p.R188C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000389048
Start 29532108:29532108(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.961C>A
AA Mutation p.Leu321Ile(p.L321I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000389048
Start 29193768:29193768(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4319C>T
AA Mutation p.Ala1440Val(p.A1440V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 28
Mutation Consequence missense_variant
Transcription ID ENST00000389048
Start 29275110:29275110(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2030T>G
AA Mutation p.Phe677Cys(p.F677C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 29
Mutation Consequence missense_variant
Transcription ID ENST00000389048
Start 29920214:29920214(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs374276783
CDS Mutation c.446C>T
AA Mutation p.Ala149Val(p.A149V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 30
Mutation Consequence synonymous_variant
Transcription ID ENST00000389048
Start 29251176:29251176(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs77102810
CDS Mutation c.2133C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 31
Mutation Consequence synonymous_variant
Transcription ID ENST00000389048
Start 29296953:29296953(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs367912697
CDS Mutation c.1752C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 32
Mutation Consequence synonymous_variant
Transcription ID ENST00000389048
Start 29694920:29694920(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.882C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 33
Mutation Consequence synonymous_variant
Transcription ID ENST00000389048
Start 29223364:29223364(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3337C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 34
Mutation Consequence synonymous_variant
Transcription ID ENST00000389048
Start 29251116:29251116(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs56017149
CDS Mutation c.2193C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 35
Mutation Consequence synonymous_variant
Transcription ID ENST00000389048
Start 29383835:29383835(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs371642412
CDS Mutation c.1179C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 36
Mutation Consequence synonymous_variant
Transcription ID ENST00000389048
Start 29275484:29275484(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1830G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 37
Mutation Consequence synonymous_variant
Transcription ID ENST00000389048
Start 29717609:29717609(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.756C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 38
Mutation Consequence synonymous_variant
Transcription ID ENST00000389048
Start 29296902:29296902(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs769055778
CDS Mutation c.1803C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 39
Mutation Consequence synonymous_variant
Transcription ID ENST00000389048
Start 29193503:29193503(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs746470148
CDS Mutation c.4584C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 40
Mutation Consequence synonymous_variant
Transcription ID ENST00000389048
Start 29920441:29920441(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.219G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 41
Mutation Consequence synonymous_variant
Transcription ID ENST00000389048
Start 29193704:29193704(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4383C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 42
Mutation Consequence synonymous_variant
Transcription ID ENST00000389048
Start 29275454:29275454(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1860A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 43
Mutation Consequence synonymous_variant
Transcription ID ENST00000389048
Start 29196773:29196773(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4161C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 44
Mutation Consequence synonymous_variant
Transcription ID ENST00000389048
Start 29193455:29193455(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4632C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 45
Mutation Consequence frameshift_variant
Transcription ID ENST00000389048
Start 29228957:29228957(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2742delG
AA Mutation p.Trp915GlyfsTer24(p.W915Gfs*24)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 46
Mutation Consequence frameshift_variant
Transcription ID ENST00000389048
Start 29228977:29228977(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2722delC
AA Mutation p.Gln908ArgfsTer3(p.Q908Rfs*3)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 47
Mutation Consequence stop_gained
Transcription ID ENST00000389048
Start 29328407:29328407(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1357C>T
AA Mutation p.Gln453Ter(p.Q453*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 48
Mutation Consequence stop_gained
Transcription ID ENST00000389048
Start 29383813:29383813(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1201C>T
AA Mutation p.Arg401Ter(p.R401*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 49
Mutation Consequence frameshift_variant
Transcription ID ENST00000389048
Start 29275455:29275456(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1858_1859insT
AA Mutation p.Arg620MetfsTer7(p.R620Mfs*7)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript

Rectum Cancer: Gene >> ALK

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000389048
Start 29320862:29320862(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1435T>G
AA Mutation p.Tyr479Asp(p.Y479D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000389048
Start 29383756:29383756(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1258T>C
AA Mutation p.Phe420Leu(p.F420L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000389048
Start 29232357:29232357(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2579G>T
AA Mutation p.Arg860Ile(p.R860I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000389048
Start 29531944:29531944(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1125C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000389048
Start 29193335:29193335(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs758556216
CDS Mutation c.4752C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000389048
Start 29239797:29239797(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs142109683
CDS Mutation c.2238C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000389048
Start 29383739:29383739(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1275C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 8
Mutation Consequence stop_gained
Transcription ID ENST00000389048
Start 29383813:29383813(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1201C>T
AA Mutation p.Arg401Ter(p.R401*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence stop_gained
Transcription ID ENST00000389048
Start 29220726:29220726(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs769449619
CDS Mutation c.3625C>T
AA Mutation p.Arg1209Ter(p.R1209*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript