Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> AXIN2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000307078
Start	65541498:65541498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1016G>A
AA Mutation	p.Arg339His(p.R339H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000307078
Start	65558436:65558436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.185T>C
AA Mutation	p.Leu62Ser(p.L62S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000307078
Start	65558427:65558427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.194C>T
AA Mutation	p.Pro65Leu(p.P65L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000307078
Start	65537507:65537507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367938045
CDS Mutation	c.1529C>T
AA Mutation	p.Thr510Met(p.T510M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000307078
Start	65558493:65558493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.128G>A
AA Mutation	p.Gly43Asp(p.G43D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000307078
Start	65558091:65558091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.530A>C
AA Mutation	p.Glu177Ala(p.E177A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000307078
Start	65537732:65537732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1304C>T
AA Mutation	p.Pro435Leu(p.P435L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000307078
Start	65536449:65536449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765845684
CDS Mutation	c.2012G>A
AA Mutation	p.Arg671His(p.R671H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000307078
Start	65537504:65537504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200883019
CDS Mutation	c.1532C>T
AA Mutation	p.Thr511Met(p.T511M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000307078
Start	65537784:65537784(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1252C>T
AA Mutation	p.Pro418Ser(p.P418S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000307078
Start	65537796:65537796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751229839
CDS Mutation	c.1240C>T
AA Mutation	p.Arg414Trp(p.R414W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307078
Start	65558522:65558522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.99C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307078
Start	65537785:65537785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs557397475
CDS Mutation	c.1251G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307078
Start	65537467:65537467(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745968863
CDS Mutation	c.1569C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307078
Start	65536382:65536382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2079G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307078
Start	65537821:65537822(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs771001164
CDS Mutation	c.1214_1215delAG
AA Mutation	p.Glu405GlyfsTer56(p.E405Gfs*56)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307078
Start	65536450:65536450(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2011delC
AA Mutation	p.Arg671AlafsTer18(p.R671Afs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307078
Start	65536467:65536467(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs267606674
CDS Mutation	c.1994delG
AA Mutation	p.Gly665AlafsTer24(p.G665Afs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307078
Start	65558049:65558049(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.572delT
AA Mutation	p.Leu191Ter(p.L191*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307078
Start	65537787:65537787(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1249delG
AA Mutation	p.Ala417ArgfsTer41(p.A417Rfs*41)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307078
Start	65558332:65558333(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.288_289delAA
AA Mutation	p.Thr97PhefsTer43(p.T97Ffs*43)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307078
Start	65558231:65558247(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.374_390delCCAAAACTTTACGAGTA
AA Mutation	p.Thr125SerfsTer10(p.T125Sfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307078
Start	65536399:65536399(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2062delC
AA Mutation	p.Leu688Ter(p.L688*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307078
Start	65537820:65537821(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1214_1215dupAG
AA Mutation	p.Gly406ArgfsTer53(p.G406Rfs*53)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307078
Start	65537540:65537541(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1495dupC
AA Mutation	p.Leu499ProfsTer129(p.L499Pfs*129)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307078
Start	65536466:65536467(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs747355609
CDS Mutation	c.1994dupG
AA Mutation	p.Asn666GlnfsTer41(p.N666Qfs*41)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307078
Start	65558476:65558477(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.143_144dupCC
AA Mutation	p.Met49ProfsTer28(p.M49Pfs*28)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307078
Start	65549602:65549603(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.873dupT
AA Mutation	p.Ala292CysfsTer10(p.A292Cfs*10)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307078
Start	65557856:65557857(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.764dupT
AA Mutation	p.Arg256GlufsTer13(p.R256Efs*13)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307078
Start	65541469:65541470(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1044dupT
AA Mutation	p.Leu349SerfsTer25(p.L349Sfs*25)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307078
Start	65549570:65549571(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.905dupT
AA Mutation	p.Ser303IlefsTer3(p.S303Ifs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307078
Start	65536398:65536399(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2062dupC
AA Mutation	p.Leu688ProfsTer19(p.L688Pfs*19)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	splice_donor_variant;coding_sequence_variant;intron_variant
Transcription ID	ENST00000307078
Start	65549512:65549520(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.956_956+8delTGTGAGTAT
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> AXIN2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000307078
Start	65558280:65558280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.341G>T
AA Mutation	p.Cys114Phe(p.C114F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000307078
Start	65557909:65557909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.712G>C
AA Mutation	p.Asp238His(p.D238H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000307078
Start	65558058:65558058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.563A>C
AA Mutation	p.Gln188Pro(p.Q188P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000307078
Start	65558052:65558052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.569T>G
AA Mutation	p.Phe190Cys(p.F190C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307078
Start	65558609:65558609(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.12delT
AA Mutation	p.Met5CysfsTer3(p.M5Cfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307078
Start	65558290:65558290(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.331delT
AA Mutation	p.Trp111GlyfsTer10(p.W111Gfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript