Colon Cancer: Gene >> SULT2B1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000201586
Start	48587376:48587376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.362T>C
AA Mutation	p.Leu121Pro(p.L121P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000201586
Start	48587279:48587279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.265C>A
AA Mutation	p.Pro89Thr(p.P89T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000201586
Start	48599359:48599359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1051C>A
AA Mutation	p.Pro351Thr(p.P351T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000201586
Start	48587394:48587394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.380C>T
AA Mutation	p.Pro127Leu(p.P127L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SULT2B1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000201586
Start	48599187:48599187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780816664
CDS Mutation	c.879C>T
Mutation Classification	Silent
Feature Type	Transcript