Colon Cancer: Gene >> CMTR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000338099
Start	71285065:71285065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.856A>C
AA Mutation	p.Asn286His(p.N286H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000338099
Start	71284164:71284164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1757C>T
AA Mutation	p.Ser586Leu(p.S586L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000338099
Start	71285370:71285370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.551T>G
AA Mutation	p.Leu184Arg(p.L184R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000338099
Start	71283833:71283833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2088T>A
AA Mutation	p.Asn696Lys(p.N696K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338099
Start	71284064:71284064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1857T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338099
Start	71284625:71284625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1296A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338099
Start	71285012:71285012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.909T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000338099
Start	71285840:71285840(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.81delT
AA Mutation	p.Phe27LeufsTer40(p.F27Lfs*40)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000338099
Start	71284123:71284123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200221398
CDS Mutation	c.1798C>T
AA Mutation	p.Arg600Ter(p.R600*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000338099
Start	71284667:71284667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1254G>A
AA Mutation	p.Trp418Ter(p.W418*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000338099
Start	71284269:71284270(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1651dupT
AA Mutation	p.Ser551PhefsTer2(p.S551Ffs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CMTR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000338099
Start	71285330:71285330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.591G>C
AA Mutation	p.Leu197Phe(p.L197F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000338099
Start	71284701:71284701(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1220A>C
AA Mutation	p.Lys407Thr(p.K407T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000338099
Start	71285720:71285720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.201G>T
AA Mutation	p.Lys67Asn(p.K67N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338099
Start	71284085:71284085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1836T>C
Mutation Classification	Silent
Feature Type	Transcript