Colon Cancer: Gene >> CCNT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261900
Start	48701053:48701053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.393A>T
AA Mutation	p.Gln131His(p.Q131H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261900
Start	48694399:48694399(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs575488596
CDS Mutation	c.815G>A
AA Mutation	p.Arg272Gln(p.R272Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261900
Start	48716549:48716549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.127A>G
AA Mutation	p.Asn43Asp(p.N43D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261900
Start	48693221:48693221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1993C>A
AA Mutation	p.His665Asn(p.H665N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261900
Start	48694249:48694249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.965A>G
AA Mutation	p.Asn322Ser(p.N322S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000261900
Start	48694034:48694034(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1180G>A
AA Mutation	p.Ala394Thr(p.A394T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000261900
Start	48695775:48695775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.761G>A
AA Mutation	p.Arg254His(p.R254H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261900
Start	48693687:48693687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1527G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261900
Start	48693216:48693216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1998C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261900
Start	48694167:48694167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1047T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000261900
Start	48694043:48694043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1171G>T
AA Mutation	p.Glu391Ter(p.E391*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000261900
Start	48693998:48693998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1216C>T
AA Mutation	p.Gln406Ter(p.Q406*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CCNT1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261900
Start	48693303:48693303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776473833
CDS Mutation	c.1911G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261900
Start	48694224:48694224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.990G>A
Mutation Classification	Silent
Feature Type	Transcript