Colon Cancer: Gene >> BCR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000305877
Start	23311783:23311783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3269G>A
AA Mutation	p.Arg1090His(p.R1090H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000305877
Start	23287265:23287265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2513G>A
AA Mutation	p.Ser838Asn(p.S838N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000305877
Start	23285062:23285062(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs182714218
CDS Mutation	c.2267A>G
AA Mutation	p.Tyr756Cys(p.Y756C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000305877
Start	23273111:23273111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770962732
CDS Mutation	c.1952C>T
AA Mutation	p.Thr651Met(p.T651M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000305877
Start	23295136:23295136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2993T>C
AA Mutation	p.Met998Thr(p.M998T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000305877
Start	23295124:23295124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs550045049
CDS Mutation	c.2981C>T
AA Mutation	p.Thr994Met(p.T994M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000305877
Start	23271572:23271572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201579887
CDS Mutation	c.1901C>T
AA Mutation	p.Thr634Met(p.T634M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000305877
Start	23285038:23285038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs189814131
CDS Mutation	c.2243C>T
AA Mutation	p.Thr748Met(p.T748M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000305877
Start	23181939:23181939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.979G>A
AA Mutation	p.Gly327Ser(p.G327S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000305877
Start	23311785:23311785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778229520
CDS Mutation	c.3271G>A
AA Mutation	p.Val1091Met(p.V1091M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000305877
Start	23285053:23285053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2258G>A
AA Mutation	p.Cys753Tyr(p.C753Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000305877
Start	23268427:23268427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1772A>G
AA Mutation	p.Tyr591Cys(p.Y591C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000305877
Start	23268486:23268486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1831G>A
AA Mutation	p.Ala611Thr(p.A611T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000305877
Start	23181445:23181445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.485G>A
AA Mutation	p.Arg162His(p.R162H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305877
Start	23314570:23314570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3582A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305877
Start	23311829:23311829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760855238
CDS Mutation	c.3315C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305877
Start	23181842:23181842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.882C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305877
Start	23273747:23273747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs532000140
CDS Mutation	c.2088G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305877
Start	23181932:23181932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.972C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305877
Start	23314015:23314015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3505C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305877
Start	23295041:23295041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2898G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305877
Start	23253908:23253908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs547409270
CDS Mutation	c.1389G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305877
Start	23295113:23295113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780726729
CDS Mutation	c.2970C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305877
Start	23181491:23181491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143556635
CDS Mutation	c.531C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	stop_gained
Transcription ID	ENST00000305877
Start	23289552:23289552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2638C>T
AA Mutation	p.Gln880Ter(p.Q880*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000305877
Start	23273134:23273134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1974+1G>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> BCR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000305877
Start	23273695:23273695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760268025
CDS Mutation	c.2036G>A
AA Mutation	p.Arg679His(p.R679H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000305877
Start	23284037:23284037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2176C>T
AA Mutation	p.Arg726Cys(p.R726C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000305877
Start	23292565:23292565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2807A>G
AA Mutation	p.Asp936Gly(p.D936G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305877
Start	23261480:23261480(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1692C>A
Mutation Classification	Silent
Feature Type	Transcript