Colon Cancer: Gene >> EZH2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000460911
Start	148814050:148814050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1745C>T
AA Mutation	p.Pro582Leu(p.P582L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000460911
Start	148807682:148807682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2205G>T
AA Mutation	p.Lys735Asn(p.K735N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000460911
Start	148828858:148828858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.507A>C
AA Mutation	p.Glu169Asp(p.E169D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000460911
Start	148818017:148818017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1085G>A
AA Mutation	p.Ser362Asn(p.S362N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000460911
Start	148814035:148814035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1760C>T
AA Mutation	p.Thr587Ile(p.T587I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000460911
Start	148814080:148814080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1715C>T
AA Mutation	p.Pro572Leu(p.P572L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000460911
Start	148827254:148827254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377467108
CDS Mutation	c.638G>A
AA Mutation	p.Arg213His(p.R213H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000460911
Start	148826616:148826616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.745G>A
AA Mutation	p.Glu249Lys(p.E249K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000460911
Start	148846597:148846597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.119G>T
AA Mutation	p.Ser40Ile(p.S40I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000460911
Start	148807669:148807669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs397515548
CDS Mutation	c.2218G>A
AA Mutation	p.Glu740Lys(p.E740K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000460911
Start	148814069:148814069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1726G>A
AA Mutation	p.Ala576Thr(p.A576T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000460911
Start	148809093:148809093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747933788
CDS Mutation	c.2158G>A
AA Mutation	p.Glu720Lys(p.E720K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000460911
Start	148819669:148819669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.911A>G
AA Mutation	p.Asn304Ser(p.N304S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000460911
Start	148828813:148828813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773610876
CDS Mutation	c.552T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000460911
Start	148829768:148829768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.444A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000460911
Start	148809362:148809362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2043T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000460911
Start	148817896:148817896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1206T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000460911
Start	148811700:148811700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1857T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000460911
Start	148826557:148826557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.804T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000460911
Start	148847224:148847224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.75A>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> EZH2

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000460911
Start	148847281:148847281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.18G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000460911
Start	148826512:148826512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.849G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000460911
Start	148818079:148818079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1023G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000460911
Start	148809078:148809079(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2172dupT
AA Mutation	p.Asp725Ter(p.D725*)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000460911
Start	148811721:148811721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1837-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript