Colon Cancer: Gene >> SPOCK1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000394945
Start	136992580:136992580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201506391
CDS Mutation	c.610C>T
AA Mutation	p.Arg204Trp(p.R204W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000394945
Start	137140611:137140611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.316C>A
AA Mutation	p.Leu106Met(p.L106M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000394945
Start	136992565:136992565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756110717
CDS Mutation	c.625C>T
AA Mutation	p.Arg209Trp(p.R209W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000394945
Start	136992592:136992592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.598G>T
AA Mutation	p.Asp200Tyr(p.D200Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394945
Start	137067806:137067806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.498T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000394945
Start	136988615:136988615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.735C>A
AA Mutation	p.Cys245Ter(p.C245*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SPOCK1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394945
Start	136978669:136978669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs531191446
CDS Mutation	c.1305C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394945
Start	137112516:137112516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144155642
CDS Mutation	c.393G>A
Mutation Classification	Silent
Feature Type	Transcript