Colon Cancer: Gene >> TH

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000381178
Start	2166759:2166759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.944G>A
AA Mutation	p.Gly315Asp(p.G315D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000381178
Start	2167882:2167882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.721G>A
AA Mutation	p.Ala241Thr(p.A241T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000381178
Start	2165760:2165760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1201T>C
AA Mutation	p.Tyr401His(p.Y401H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000381178
Start	2167015:2167015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757607038
CDS Mutation	c.806C>T
AA Mutation	p.Thr269Met(p.T269M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000381178
Start	2167926:2167926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372409517
CDS Mutation	c.677C>T
AA Mutation	p.Ser226Leu(p.S226L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381178
Start	2164344:2164344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs552808212
CDS Mutation	c.1476G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381178
Start	2169794:2169794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776640286
CDS Mutation	c.261G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381178
Start	2165740:2165740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769329337
CDS Mutation	c.1221C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381178
Start	2165270:2165270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760210103
CDS Mutation	c.1389C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000381178
Start	2171775:2171775(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.12delC
AA Mutation	p.Asp5ThrfsTer27(p.D5Tfs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000381178
Start	2169649:2169649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.405+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> TH

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000381178
Start	2164328:2164328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200751977
CDS Mutation	c.1492G>A
AA Mutation	p.Asp498Asn(p.D498N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000381178
Start	2169867:2169867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746136903
CDS Mutation	c.188C>T
AA Mutation	p.Pro63Leu(p.P63L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381178
Start	2169677:2169677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749856378
CDS Mutation	c.378G>A
Mutation Classification	Silent
Feature Type	Transcript