Colon Cancer: Gene >> MTR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000366577
Start	236812758:236812758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.523G>A
AA Mutation	p.Ala175Thr(p.A175T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000366577
Start	236852597:236852597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1772G>A
AA Mutation	p.Arg591Gln(p.R591Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000366577
Start	236810581:236810581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.488A>G
AA Mutation	p.Asp163Gly(p.D163G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000366577
Start	236852988:236852988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1853C>T
AA Mutation	p.Pro618Leu(p.P618L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000366577
Start	236803548:236803548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs12749581
CDS Mutation	c.155G>A
AA Mutation	p.Arg52Gln(p.R52Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000366577
Start	236831990:236831990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773581879
CDS Mutation	c.1100C>T
AA Mutation	p.Pro367Leu(p.P367L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000366577
Start	236852988:236852988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1853C>A
AA Mutation	p.Pro618His(p.P618H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000366577
Start	236891153:236891153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3028T>C
AA Mutation	p.Tyr1010His(p.Y1010H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000366577
Start	236891252:236891252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3127G>A
AA Mutation	p.Asp1043Asn(p.D1043N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366577
Start	236889323:236889323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778549407
CDS Mutation	c.2994C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000366577
Start	236852615:236852615(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1793delT
AA Mutation	p.Phe598SerfsTer14(p.F598Sfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000366577
Start	236850378:236850378(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1552delC
AA Mutation	p.Arg518GlyfsTer7(p.R518Gfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000366577
Start	236874751:236874752(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2500dupA
AA Mutation	p.Thr834AsnfsTer6(p.T834Nfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000366577
Start	236894464:236894465(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.3315dupT
AA Mutation	p.Gly1106TrpfsTer10(p.G1106Wfs*10)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000366577
Start	236812821:236812822(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.591dupT
AA Mutation	p.Asp198Ter(p.D198*)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MTR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000366577
Start	236861189:236861189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778233369
CDS Mutation	c.2108G>A
AA Mutation	p.Arg703Gln(p.R703Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000366577
Start	236886346:236886346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2830T>A
AA Mutation	p.Trp944Arg(p.W944R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000366577
Start	236885199:236885199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2755G>A
AA Mutation	p.Asp919Asn(p.D919N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366577
Start	236889281:236889281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2952C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366577
Start	236835669:236835669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777192214
CDS Mutation	c.1311C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000366577
Start	236874724:236874724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2474-2A>T
Mutation Classification	Splice_Site
Feature Type	Transcript