Colon Cancer: Gene >> CCSAP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000284617
Start	229326853:229326853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.521C>T
AA Mutation	p.Ser174Leu(p.S174L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000284617
Start	229326752:229326752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.622G>A
AA Mutation	p.Ala208Thr(p.A208T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000284617
Start	229326757:229326757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.617C>T
AA Mutation	p.Ala206Val(p.A206V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000284617
Start	229342403:229342403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.63G>T
AA Mutation	p.Glu21Asp(p.E21D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284617
Start	229325247:229325247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.801G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284617
Start	229326882:229326882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.492G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CCSAP

Mutation ID	1
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000284617
Start	229326959:229326959(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.415delA
AA Mutation	p.Thr139GlnfsTer39(p.T139Qfs*39)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript