Colon Cancer: Gene >> CDC27

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000066544
Start	47122492:47122492(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2344C>T
AA Mutation	p.Arg782Cys(p.R782C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000066544
Start	47171951:47171951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.217T>C
AA Mutation	p.Tyr73His(p.Y73H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000066544
Start	47181583:47181583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.82G>A
AA Mutation	p.Ala28Thr(p.A28T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000066544
Start	47122548:47122548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2288C>T
AA Mutation	p.Ala763Val(p.A763V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000066544
Start	47169959:47169959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.335A>G
AA Mutation	p.Asp112Gly(p.D112G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000066544
Start	47138746:47138746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1697C>T
AA Mutation	p.Ser566Leu(p.S566L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000066544
Start	47181592:47181592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.73G>T
AA Mutation	p.Val25Phe(p.V25F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000066544
Start	47143978:47143978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1075A>T
AA Mutation	p.Thr359Ser(p.T359S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000066544
Start	47172027:47172027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.141T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000066544
Start	47142397:47142397(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1210delA
AA Mutation	p.Ile404SerfsTer15(p.I404Sfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000066544
Start	47171986:47171986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.182T>A
AA Mutation	p.Leu61Ter(p.L61*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000066544
Start	47143976:47143977(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1076_1077insTTTAAATT
AA Mutation	p.Pro360LeufsTer7(p.P360Lfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CDC27

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000066544
Start	47138746:47138746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1697C>T
AA Mutation	p.Ser566Leu(p.S566L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000066544
Start	47129502:47129502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2051A>C
AA Mutation	p.Lys684Thr(p.K684T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000066544
Start	47137298:47137298(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1767C>A
AA Mutation	p.Phe589Leu(p.F589L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000066544
Start	47156933:47156933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.822T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000066544
Start	47123915:47123915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2206G>T
AA Mutation	p.Glu736Ter(p.E736*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript