Colon Cancer: Gene >> WNT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265441
Start	117315223:117315223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.436A>G
AA Mutation	p.Lys146Glu(p.K146E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265441
Start	117315151:117315151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377188020
CDS Mutation	c.508G>A
AA Mutation	p.Ala170Thr(p.A170T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265441
Start	117278179:117278179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146785086
CDS Mutation	c.1059C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265441
Start	117315152:117315152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370359868
CDS Mutation	c.507C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265441
Start	117320720:117320721(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.156_157delGC
AA Mutation	p.Gln53AlafsTer13(p.Q53Afs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000265441
Start	117320708:117320708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.169C>T
AA Mutation	p.Arg57Ter(p.R57*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265441
Start	117315335:117315336(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.323_324insAAAAA
AA Mutation	p.Ala109LysfsTer26(p.A109Kfs*26)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> WNT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265441
Start	117278241:117278241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779778873
CDS Mutation	c.997G>A
AA Mutation	p.Ala333Thr(p.A333T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265441
Start	117315101:117315101(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.558G>T
AA Mutation	p.Met186Ile(p.M186I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265441
Start	117322974:117322974(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769047659
CDS Mutation	c.16G>A
AA Mutation	p.Gly6Ser(p.G6S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265441
Start	117320650:117320650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.227G>A
AA Mutation	p.Cys76Tyr(p.C76Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265441
Start	117278238:117278238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1000G>A
AA Mutation	p.Val334Met(p.V334M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265441
Start	117315084:117315084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.575G>T
AA Mutation	p.Arg192Ile(p.R192I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265441
Start	117322927:117322927(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.63delC
AA Mutation	p.Glu22ArgfsTer9(p.E22Rfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript