Colon Cancer: Gene >> EZH1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000428826
Start	42705114:42705114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1909G>A
AA Mutation	p.Glu637Lys(p.E637K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000428826
Start	42706041:42706041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1805G>A
AA Mutation	p.Cys602Tyr(p.C602Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000428826
Start	42720383:42720383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.554A>T
AA Mutation	p.Gln185Leu(p.Q185L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000428826
Start	42706020:42706020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748173627
CDS Mutation	c.1826G>A
AA Mutation	p.Arg609His(p.R609H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000428826
Start	42706052:42706052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1794G>T
AA Mutation	p.Lys598Asn(p.K598N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000428826
Start	42703784:42703784(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2054T>A
AA Mutation	p.Ile685Asn(p.I685N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000428826
Start	42708036:42708036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1582G>T
AA Mutation	p.Asp528Tyr(p.D528Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000428826
Start	42708046:42708046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs573197442
CDS Mutation	c.1572C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000428826
Start	42706175:42706175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1671T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000428826
Start	42703798:42703799(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2039_2040delGG
AA Mutation	p.Arg680GlnfsTer46(p.R680Qfs*46)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained;protein_altering_variant
Transcription ID	ENST00000428826
Start	42703796:42703797(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2041_2042insGCT
AA Mutation	p.Lys681delinsSerTer(p.K681delinsS*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained;frameshift_variant
Transcription ID	ENST00000428826
Start	42718590:42718591(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.794_795insGTAG
AA Mutation	p.Asp265GlufsTer2(p.D265Efs*2)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> EZH1

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000428826
Start	42703782:42703782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2056C>T
AA Mutation	p.Arg686Ter(p.R686*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000428826
Start	42712363:42712363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1327C>T
AA Mutation	p.Arg443Ter(p.R443*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript