Colon Cancer: Gene >> NEO1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261908
Start	73126558:73126558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.866T>C
AA Mutation	p.Leu289Pro(p.L289P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261908
Start	73116711:73116711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769006214
CDS Mutation	c.302G>A
AA Mutation	p.Arg101His(p.R101H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261908
Start	73301380:73301380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4225C>T
AA Mutation	p.Arg1409Trp(p.R1409W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261908
Start	73116807:73116807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.398T>C
AA Mutation	p.Val133Ala(p.V133A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261908
Start	73258796:73258796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778980899
CDS Mutation	c.2123G>A
AA Mutation	p.Arg708Gln(p.R708Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000261908
Start	73116624:73116624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.215T>C
AA Mutation	p.Leu72Ser(p.L72S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000261908
Start	73260277:73260277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766139025
CDS Mutation	c.2210G>A
AA Mutation	p.Arg737His(p.R737H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000261908
Start	73249695:73249695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1868A>G
AA Mutation	p.Asp623Gly(p.D623G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000261908
Start	73178365:73178365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1229G>A
AA Mutation	p.Cys410Tyr(p.C410Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000261908
Start	73298578:73298578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4132G>A
AA Mutation	p.Ala1378Thr(p.A1378T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000261908
Start	73288482:73288482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3580T>G
AA Mutation	p.Ser1194Ala(p.S1194A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000261908
Start	73298393:73298393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3947C>T
AA Mutation	p.Ser1316Leu(p.S1316L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000261908
Start	73270381:73270381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2784C>A
AA Mutation	p.Phe928Leu(p.F928L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261908
Start	73270143:73270143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2628C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261908
Start	73122628:73122628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.552G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261908
Start	73260401:73260401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2334C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261908
Start	73126529:73126529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.837C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261908
Start	73236429:73236429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763026515
CDS Mutation	c.1374G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000261908
Start	73298356:73298356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3910C>T
AA Mutation	p.Arg1304Ter(p.R1304*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000261908
Start	73288536:73288536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3634C>T
AA Mutation	p.Arg1212Ter(p.R1212*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000261908
Start	73289239:73289239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747725504
CDS Mutation	c.3742+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> NEO1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261908
Start	73116687:73116687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.278T>C
AA Mutation	p.Leu93Ser(p.L93S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261908
Start	73135935:73135935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.923G>C
AA Mutation	p.Ser308Thr(p.S308T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261908
Start	73249707:73249707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368526754
CDS Mutation	c.1880G>A
AA Mutation	p.Arg627Gln(p.R627Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261908
Start	73254789:73254789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2052G>T
AA Mutation	p.Glu684Asp(p.E684D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261908
Start	73176543:73176543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1156T>C
AA Mutation	p.Tyr386His(p.Y386H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000261908
Start	73298356:73298356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3910C>T
AA Mutation	p.Arg1304Ter(p.R1304*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000261908
Start	73301320:73301320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4166-1G>C
Mutation Classification	Splice_Site
Feature Type	Transcript