Colon Cancer: Gene >> WBP4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379487
Start	41062661:41062661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.20C>T
AA Mutation	p.Ser7Leu(p.S7L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000379487
Start	41080677:41080677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.788A>C
AA Mutation	p.Asp263Ala(p.D263A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000379487
Start	41068663:41068663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.365A>C
AA Mutation	p.Asp122Ala(p.D122A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000379487
Start	41082829:41082829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1046C>T
AA Mutation	p.Ala349Val(p.A349V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000379487
Start	41065042:41065042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.102G>T
AA Mutation	p.Lys34Asn(p.K34N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000379487
Start	41065224:41065224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.199G>T
AA Mutation	p.Ala67Ser(p.A67S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379487
Start	41065268:41065268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.243A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000379487
Start	41082875:41082875(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1095delA
AA Mutation	p.Lys365AsnfsTer5(p.K365Nfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000379487
Start	41068655:41068655(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.363delA
AA Mutation	p.Asp122IlefsTer8(p.D122Ifs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000379487
Start	41082798:41082799(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1021dupA
AA Mutation	p.Thr341AsnfsTer22(p.T341Nfs*22)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000379487
Start	41065163:41065163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.139-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> WBP4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379487
Start	41082814:41082814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367965408
CDS Mutation	c.1031C>T
AA Mutation	p.Ser344Phe(p.S344F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000379487
Start	41062686:41062686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.45C>A
AA Mutation	p.Tyr15Ter(p.Y15*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript