Colon Cancer: Gene >> CPD

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000225719
Start	30420852:30420852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1006G>A
AA Mutation	p.Asp336Asn(p.D336N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000225719
Start	30442425:30442425(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2348G>T
AA Mutation	p.Arg783Ile(p.R783I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000225719
Start	30445773:30445773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2626G>T
AA Mutation	p.Asp876Tyr(p.D876Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000225719
Start	30423542:30423542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1694G>A
AA Mutation	p.Gly565Glu(p.G565E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000225719
Start	30379175:30379175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.195G>T
AA Mutation	p.Glu65Asp(p.E65D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000225719
Start	30379177:30379177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.197C>T
AA Mutation	p.Ser66Leu(p.S66L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000225719
Start	30427481:30427481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1940C>A
AA Mutation	p.Pro647His(p.P647H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000225719
Start	30427502:30427502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1961C>T
AA Mutation	p.Ala654Val(p.A654V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000225719
Start	30456511:30456511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3483C>A
AA Mutation	p.His1161Gln(p.H1161Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000225719
Start	30422756:30422756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1390A>G
AA Mutation	p.Thr464Ala(p.T464A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000225719
Start	30449669:30449669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2990C>T
AA Mutation	p.Ala997Val(p.A997V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000225719
Start	30449706:30449706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3027A>T
AA Mutation	p.Glu1009Asp(p.E1009D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000225719
Start	30445816:30445816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2669G>C
AA Mutation	p.Ser890Thr(p.S890T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000225719
Start	30422880:30422880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1514A>C
AA Mutation	p.His505Pro(p.H505P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000225719
Start	30461212:30461212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3531A>C
AA Mutation	p.Glu1177Asp(p.E1177D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000225719
Start	30427453:30427453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1912C>A
AA Mutation	p.Pro638Thr(p.P638T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000225719
Start	30461982:30461982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3736G>T
AA Mutation	p.Gly1246Cys(p.G1246C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000225719
Start	30427552:30427552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2011C>T
AA Mutation	p.His671Tyr(p.H671Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000225719
Start	30385160:30385160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.918G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000225719
Start	30385157:30385157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.915T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000225719
Start	30423010:30423010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1644T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000225719
Start	30464664:30464664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3993G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000225719
Start	30422956:30422956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1590A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000225719
Start	30445820:30445820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2673C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000225719
Start	30422763:30422764(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1399dupA
AA Mutation	p.Ile467AsnfsTer3(p.I467Nfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CPD

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000225719
Start	30462431:30462431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3878T>G
AA Mutation	p.Ile1293Arg(p.I1293R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000225719
Start	30423666:30423666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1818G>T
AA Mutation	p.Met606Ile(p.M606I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000225719
Start	30423694:30423694(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1846G>A
AA Mutation	p.Glu616Lys(p.E616K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000225719
Start	30449678:30449678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2999G>A
AA Mutation	p.Gly1000Glu(p.G1000E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript