Colon Cancer: Gene >> TREH

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264029
Start	118661175:118661175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.842C>A
AA Mutation	p.Pro281His(p.P281H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264029
Start	118658918:118658918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1532C>T
AA Mutation	p.Ala511Val(p.A511V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264029
Start	118659789:118659789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1278C>A
AA Mutation	p.Phe426Leu(p.F426L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000264029
Start	118662968:118662968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.336C>A
AA Mutation	p.Ser112Arg(p.S112R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264029
Start	118662930:118662930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs573986675
CDS Mutation	c.374G>A
AA Mutation	p.Arg125His(p.R125H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000264029
Start	118659875:118659875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1192G>T
AA Mutation	p.Ala398Ser(p.A398S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000264029
Start	118660691:118660691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.950A>G
AA Mutation	p.Glu317Gly(p.E317G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000264029
Start	118661960:118661960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782513341
CDS Mutation	c.454C>T
AA Mutation	p.Arg152Trp(p.R152W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000264029
Start	118659402:118659402(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1400C>T
AA Mutation	p.Ala467Val(p.A467V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264029
Start	118659951:118659951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1116G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264029
Start	118662964:118662964(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.340delC
AA Mutation	p.Gln114SerfsTer29(p.Q114Sfs*29)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000264029
Start	118659746:118659746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1320+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> TREH

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264029
Start	118659934:118659934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1133T>G
AA Mutation	p.Ile378Ser(p.I378S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript