Colon Cancer: Gene >> SULT4A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000330884
Start	43862241:43862241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.142G>A
AA Mutation	p.Val48Met(p.V48M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000330884
Start	43826081:43826081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374057069
CDS Mutation	c.775G>A
AA Mutation	p.Val259Ile(p.V259I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000330884
Start	43833726:43833726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.517G>A
AA Mutation	p.Gly173Ser(p.G173S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000330884
Start	43841870:43841870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.232G>T
AA Mutation	p.Gly78Cys(p.G78C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000330884
Start	43862259:43862259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.124C>A
AA Mutation	p.Pro42Thr(p.P42T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000330884
Start	43829112:43829112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.690C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000330884
Start	43862338:43862338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.45C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SULT4A1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000330884
Start	43862323:43862323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769978752
CDS Mutation	c.60C>T
Mutation Classification	Silent
Feature Type	Transcript