Colon Cancer: Gene >> DOT1L

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000398665
Start	2216762:2216762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756193932
CDS Mutation	c.2405C>T
AA Mutation	p.Ser802Leu(p.S802L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000398665
Start	2226247:2226247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3726G>C
AA Mutation	p.Lys1242Asn(p.K1242N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000398665
Start	2213957:2213957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371142941
CDS Mutation	c.1768C>T
AA Mutation	p.Arg590Cys(p.R590C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000398665
Start	2185862:2185862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.133T>G
AA Mutation	p.Cys45Gly(p.C45G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000398665
Start	2223312:2223312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3422C>T
AA Mutation	p.Thr1141Ile(p.T1141I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000398665
Start	2185889:2185889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772273572
CDS Mutation	c.160G>A
AA Mutation	p.Ala54Thr(p.A54T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000398665
Start	2213966:2213966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200802307
CDS Mutation	c.1777C>T
AA Mutation	p.Arg593Cys(p.R593C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000398665
Start	2221987:2221987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2818G>A
AA Mutation	p.Ala940Thr(p.A940T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000398665
Start	2213967:2213967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370589055
CDS Mutation	c.1778G>A
AA Mutation	p.Arg593His(p.R593H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000398665
Start	2193772:2193772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.577A>G
AA Mutation	p.Lys193Glu(p.K193E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000398665
Start	2222271:2222271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3102C>A
AA Mutation	p.Phe1034Leu(p.F1034L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000398665
Start	2206779:2206779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.838A>C
AA Mutation	p.Asn280His(p.N280H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398665
Start	2222368:2222368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3199C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398665
Start	2225436:2225436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369090875
CDS Mutation	c.3645G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398665
Start	2210824:2210824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs545805803
CDS Mutation	c.1320C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398665
Start	2206739:2206739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201441854
CDS Mutation	c.798C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000398665
Start	2199923:2199923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.691C>T
AA Mutation	p.Arg231Ter(p.R231*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> DOT1L

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398665
Start	2210764:2210764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs574510793
CDS Mutation	c.1260G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398665
Start	2194532:2194532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.606C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398665
Start	2206748:2206748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199768042
CDS Mutation	c.807G>A
Mutation Classification	Silent
Feature Type	Transcript