Colon Cancer: Gene >> WISP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000230529
Start	112068361:112068361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.746T>C
AA Mutation	p.Ile249Thr(p.I249T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000230529
Start	112064818:112064818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.410C>A
AA Mutation	p.Pro137His(p.P137H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000230529
Start	112064924:112064924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.516G>T
AA Mutation	p.Lys172Asn(p.K172N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000230529
Start	112061194:112061194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.252A>C
AA Mutation	p.Glu84Asp(p.E84D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000230529
Start	112068259:112068259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.644A>C
AA Mutation	p.Lys215Thr(p.K215T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000230529
Start	112069481:112069481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782594917
CDS Mutation	c.926A>C
AA Mutation	p.Lys309Thr(p.K309T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000230529
Start	112068372:112068372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140750750
CDS Mutation	c.757G>A
AA Mutation	p.Asp253Asn(p.D253N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000230529
Start	112068349:112068350(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.734_735insTACATATGTAT
AA Mutation	p.Arg245SerfsTer17(p.R245Sfs*17)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> WISP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000230529
Start	112069571:112069571(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1016G>T
AA Mutation	p.Arg339Ile(p.R339I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript