Colon Cancer: Gene >> HS3ST5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000312719
Start	114057390:114057390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.908A>C
AA Mutation	p.Lys303Thr(p.K303T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000312719
Start	114058083:114058083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762269276
CDS Mutation	c.215G>T
AA Mutation	p.Arg72Leu(p.R72L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000312719
Start	114057957:114057957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746548752
CDS Mutation	c.341C>T
AA Mutation	p.Pro114Leu(p.P114L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000312719
Start	114057789:114057789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.509A>G
AA Mutation	p.Tyr170Cys(p.Y170C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000312719
Start	114057354:114057354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.944A>T
AA Mutation	p.Glu315Val(p.E315V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000312719
Start	114058123:114058123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775679934
CDS Mutation	c.175C>T
AA Mutation	p.Arg59Cys(p.R59C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312719
Start	114058091:114058091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150843917
CDS Mutation	c.207C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312719
Start	114057284:114057284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778139287
CDS Mutation	c.1014C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312719
Start	114057638:114057638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61730700
CDS Mutation	c.660C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312719
Start	114062762:114062762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753747446
CDS Mutation	c.84C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000312719
Start	114057416:114057416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.882C>A
AA Mutation	p.Cys294Ter(p.C294*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> HS3ST5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000312719
Start	114057325:114057325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374141405
CDS Mutation	c.973C>T
AA Mutation	p.Arg325Cys(p.R325C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000312719
Start	114058113:114058113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.185A>G
AA Mutation	p.Gln62Arg(p.Q62R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000312719
Start	114057317:114057317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.981C>A
AA Mutation	p.Phe327Leu(p.F327L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312719
Start	114057542:114057542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.756C>A
Mutation Classification	Silent
Feature Type	Transcript