Colon Cancer: Gene >> SAG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000409110
Start	233309254:233309254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371502229
CDS Mutation	c.65G>A
AA Mutation	p.Arg22Gln(p.R22Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000409110
Start	233327164:233327164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.479G>A
AA Mutation	p.Ser160Asn(p.S160N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000409110
Start	233320657:233320657(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747018082
CDS Mutation	c.209G>A
AA Mutation	p.Arg70His(p.R70H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000409110
Start	233320680:233320680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760031511
CDS Mutation	c.232G>A
AA Mutation	p.Val78Met(p.V78M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000409110
Start	233328515:233328515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.550G>T
AA Mutation	p.Ala184Ser(p.A184S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409110
Start	233327153:233327153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375593027
CDS Mutation	c.468C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000409110
Start	233320785:233320785(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.341delA
AA Mutation	p.Lys114SerfsTer11(p.K114Sfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SAG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000409110
Start	233316099:233316099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373412387
CDS Mutation	c.100G>T
AA Mutation	p.Asp34Tyr(p.D34Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000409110
Start	233327148:233327148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745341538
CDS Mutation	c.463G>A
AA Mutation	p.Ala155Thr(p.A155T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000409110
Start	233327195:233327195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.510G>T
AA Mutation	p.Lys170Asn(p.K170N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409110
Start	233322993:233322993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.423A>G
Mutation Classification	Silent
Feature Type	Transcript