Colon Cancer: Gene >> SGCA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262018
Start	50167470:50167470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.140G>A
AA Mutation	p.Ser47Asn(p.S47N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262018
Start	50168490:50168490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199810179
CDS Mutation	c.502G>A
AA Mutation	p.Gly168Arg(p.G168R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000262018
Start	50170665:50170665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781380620
CDS Mutation	c.982G>A
AA Mutation	p.Asp328Asn(p.D328N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262018
Start	50166073:50166073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762704751
CDS Mutation	c.33C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262018
Start	50168423:50168423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763694408
CDS Mutation	c.435G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262018
Start	50175278:50175278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1005C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262018
Start	50167670:50167670(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.250delC
AA Mutation	p.His84ThrfsTer127(p.H84Tfs*127)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SGCA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262018
Start	50168409:50168409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.421C>T
AA Mutation	p.Arg141Cys(p.R141C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript