Colon Cancer: Gene >> MOCOS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261326
Start	36248987:36248987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2026G>C
AA Mutation	p.Val676Leu(p.V676L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261326
Start	36257030:36257030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2227A>G
AA Mutation	p.Asn743Asp(p.N743D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261326
Start	36195274:36195274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.160C>A
AA Mutation	p.His54Asn(p.H54N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261326
Start	36198702:36198702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373537157
CDS Mutation	c.245G>A
AA Mutation	p.Ser82Asn(p.S82N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261326
Start	36260093:36260093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776357546
CDS Mutation	c.2327G>A
AA Mutation	p.Arg776His(p.R776H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000261326
Start	36268545:36268545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747252798
CDS Mutation	c.2527A>G
AA Mutation	p.Met843Val(p.M843V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000261326
Start	36203120:36203120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.949G>T
AA Mutation	p.Asp317Tyr(p.D317Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000261326
Start	36200069:36200069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141623345
CDS Mutation	c.686C>T
AA Mutation	p.Thr229Met(p.T229M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261326
Start	36199746:36199746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376254012
CDS Mutation	c.363G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261326
Start	36195309:36195309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763082187
CDS Mutation	c.195C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant;stop_lost
Transcription ID	ENST00000261326
Start	36268684:36268684(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs755830405
CDS Mutation	c.*6delA
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> MOCOS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261326
Start	36266788:36266788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2449G>A
AA Mutation	p.Asp817Asn(p.D817N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261326
Start	36200312:36200312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs77940522
CDS Mutation	c.929C>T
AA Mutation	p.Ser310Leu(p.S310L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261326
Start	36256973:36256973(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2170C>T
AA Mutation	p.Leu724Phe(p.L724F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261326
Start	36256974:36256974(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2171T>C
AA Mutation	p.Leu724Pro(p.L724P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261326
Start	36251212:36251212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2093T>G
AA Mutation	p.Phe698Cys(p.F698C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261326
Start	36203149:36203149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs540275885
CDS Mutation	c.978C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261326
Start	36266763:36266763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2424T>C
Mutation Classification	Silent
Feature Type	Transcript