Colon Cancer: Gene >> HS3ST1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000002596
Start	11399147:11399147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370389171
CDS Mutation	c.859G>A
AA Mutation	p.Glu287Lys(p.E287K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000002596
Start	11399371:11399371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.635T>C
AA Mutation	p.Ile212Thr(p.I212T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000002596
Start	11399552:11399552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.454C>T
AA Mutation	p.Arg152Cys(p.R152C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000002596
Start	11399274:11399274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745784456
CDS Mutation	c.732G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000002596
Start	11399811:11399811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775146683
CDS Mutation	c.195C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000002596
Start	11399550:11399550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778649153
CDS Mutation	c.456C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> HS3ST1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000002596
Start	11399147:11399147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370389171
CDS Mutation	c.859G>A
AA Mutation	p.Glu287Lys(p.E287K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript