Colon Cancer: Gene >> CPSF6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000435070
Start	69260086:69260086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1358C>A
AA Mutation	p.Ser453Tyr(p.S453Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000435070
Start	69258736:69258736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.841G>A
AA Mutation	p.Gly281Arg(p.G281R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000435070
Start	69251234:69251234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.166C>A
AA Mutation	p.Leu56Ile(p.L56I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000435070
Start	69260169:69260169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1441G>A
AA Mutation	p.Glu481Lys(p.E481K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000435070
Start	69262548:69262548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1645C>T
AA Mutation	p.Arg549Cys(p.R549C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000435070
Start	69251165:69251165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.97T>C
AA Mutation	p.Tyr33His(p.Y33H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000435070
Start	69262554:69262554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1651C>T
AA Mutation	p.Arg551Cys(p.R551C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000435070
Start	69258752:69258752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.857A>G
AA Mutation	p.Gln286Arg(p.Q286R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000435070
Start	69262542:69262542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1639G>A
AA Mutation	p.Glu547Lys(p.E547K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000435070
Start	69258856:69258856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.961G>T
AA Mutation	p.Gly321Cys(p.G321C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000435070
Start	69259517:69259517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1289C>T
AA Mutation	p.Ser430Leu(p.S430L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000435070
Start	69251282:69251282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.214G>A
AA Mutation	p.Val72Ile(p.V72I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000435070
Start	69258951:69258951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765622604
CDS Mutation	c.1056G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000435070
Start	69258904:69258904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1009C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000435070
Start	69258807:69258807(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.917delC
AA Mutation	p.Pro306LeufsTer32(p.P306Lfs*32)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CPSF6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000435070
Start	69259517:69259517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1289C>T
AA Mutation	p.Ser430Leu(p.S430L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript