Colon Cancer: Gene >> SOAT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000301466
Start	53105574:53105574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.289T>A
AA Mutation	p.Ser97Thr(p.S97T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000301466
Start	53123100:53123100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759415096
CDS Mutation	c.1256G>A
AA Mutation	p.Arg419Gln(p.R419Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000301466
Start	53105571:53105571(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.286C>T
AA Mutation	p.Pro96Ser(p.P96S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000301466
Start	53115499:53115499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.553C>A
AA Mutation	p.Leu185Ile(p.L185I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000301466
Start	53123101:53123102(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1261dupG
AA Mutation	p.Val421GlyfsTer15(p.V421Gfs*15)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000301466
Start	53105106:53105106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.139-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> SOAT2

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301466
Start	53115489:53115489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs151267658
CDS Mutation	c.543G>A
Mutation Classification	Silent
Feature Type	Transcript