Colon Cancer: Gene >> AXIN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262320
Start	293545:293545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768565859
CDS Mutation	c.2129C>T
AA Mutation	p.Ala710Val(p.A710V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262320
Start	293713:293713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377025983
CDS Mutation	c.1961C>T
AA Mutation	p.Ser654Leu(p.S654L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262320
Start	293543:293543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150504240
CDS Mutation	c.2131C>T
AA Mutation	p.Arg711Cys(p.R711C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262320
Start	288177:288177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2534C>T
AA Mutation	p.Ala845Val(p.A845V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262320
Start	298134:298134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1372G>A
AA Mutation	p.Gly458Arg(p.G458R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262320
Start	304350:304350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764120241
CDS Mutation	c.1208G>A
AA Mutation	p.Arg403Gln(p.R403Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000262320
Start	304314:304314(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368340732
CDS Mutation	c.1244G>A
AA Mutation	p.Arg415His(p.R415H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000262320
Start	289513:289513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs546827136
CDS Mutation	c.2389C>T
AA Mutation	p.Arg797Cys(p.R797C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000262320
Start	304323:304323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774345751
CDS Mutation	c.1235G>A
AA Mutation	p.Arg412Gln(p.R412Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000262320
Start	346408:346408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.618T>G
AA Mutation	p.Ile206Met(p.I206M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262320
Start	346165:346165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.861C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262320
Start	346834:346834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779104449
CDS Mutation	c.192G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262320
Start	314656:314656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.906C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262320
Start	288182:288182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775437317
CDS Mutation	c.2529C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262320
Start	314605:314605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.957C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262320
Start	288227:288227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs568525212
CDS Mutation	c.2484C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262320
Start	346792:346792(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.234delC
AA Mutation	p.Thr79ProfsTer5(p.T79Pfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262320
Start	346234:346234(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.792delC
AA Mutation	p.Gly265GlufsTer149(p.G265Efs*149)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262320
Start	297089:297089(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1922delA
AA Mutation	p.Lys641ArgfsTer64(p.K641Rfs*64)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262320
Start	346962:346962(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.64delC
AA Mutation	p.Arg22AspfsTer62(p.R22Dfs*62)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262320
Start	298211:298211(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1295delC
AA Mutation	p.Pro432GlnfsTer48(p.P432Qfs*48)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000262320
Start	309972:309972(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1116+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> AXIN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262320
Start	346689:346689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.337G>A
AA Mutation	p.Asp113Asn(p.D113N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262320
Start	346965:346965(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.61C>T
AA Mutation	p.Pro21Ser(p.P21S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript