Colon Cancer: Gene >> WDPCP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000272321
Start	63433890:63433890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763859638
CDS Mutation	c.680G>A
AA Mutation	p.Arg227Gln(p.R227Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000272321
Start	63484984:63484984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.257G>A
AA Mutation	p.Arg86Gln(p.R86Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000272321
Start	63122017:63122017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2230G>A
AA Mutation	p.Gly744Ser(p.G744S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000272321
Start	63404404:63404404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141011629
CDS Mutation	c.1079C>T
AA Mutation	p.Ser360Leu(p.S360L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000272321
Start	63174829:63174829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1919T>C
AA Mutation	p.Leu640Pro(p.L640P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000272321
Start	63381909:63381909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1621G>A
AA Mutation	p.Glu541Lys(p.E541K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000272321
Start	63152943:63152943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs563554007
CDS Mutation	c.2161G>A
AA Mutation	p.Gly721Arg(p.G721R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000272321
Start	63313261:63313261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375036014
CDS Mutation	c.1799G>A
AA Mutation	p.Arg600His(p.R600H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000272321
Start	63404516:63404516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs545767612
CDS Mutation	c.967C>T
AA Mutation	p.Arg323Trp(p.R323W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000272321
Start	63492920:63492920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.96T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000272321
Start	63484968:63484968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370579497
CDS Mutation	c.273G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000272321
Start	63404470:63404470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1013C>A
AA Mutation	p.Ser338Ter(p.S338*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000272321
Start	63382029:63382030(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1500_1501insTATATACAAAACTC
AA Mutation	p.Ile501TyrfsTer10(p.I501Yfs*10)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> WDPCP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000272321
Start	63487453:63487453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.202C>A
AA Mutation	p.Pro68Thr(p.P68T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000272321
Start	63259372:63259372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780498393
CDS Mutation	c.1850C>T
AA Mutation	p.Ala617Val(p.A617V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000272321
Start	63174746:63174746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2002C>T
AA Mutation	p.Pro668Ser(p.P668S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000272321
Start	63404458:63404458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1025G>A
AA Mutation	p.Ser342Asn(p.S342N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000272321
Start	63153568:63153568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2085A>C
Mutation Classification	Silent
Feature Type	Transcript