Colon Cancer: Gene >> HS3ST4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000331351
Start	26136132:26136132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1255C>T
AA Mutation	p.Arg419Cys(p.R419C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000331351
Start	26135973:26135973(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1096G>A
AA Mutation	p.Gly366Arg(p.G366R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000331351
Start	26135872:26135872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.995G>A
AA Mutation	p.Arg332Gln(p.R332Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000331351
Start	26136121:26136121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753467285
CDS Mutation	c.1244G>A
AA Mutation	p.Arg415Gln(p.R415Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000331351
Start	26136024:26136024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1147G>C
AA Mutation	p.Glu383Gln(p.E383Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000331351
Start	25693091:25693091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.674C>T
AA Mutation	p.Ala225Val(p.A225V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000331351
Start	26136175:26136175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1298A>G
AA Mutation	p.Lys433Arg(p.K433R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000331351
Start	26136215:26136215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1338T>G
AA Mutation	p.Asp446Glu(p.D446E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331351
Start	26135801:26135801(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.924C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331351
Start	26136014:26136014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1137T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> HS3ST4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000331351
Start	25692869:25692869(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.452C>T
AA Mutation	p.Thr151Met(p.T151M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000331351
Start	26135740:26135740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.863G>T
AA Mutation	p.Arg288Ile(p.R288I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000331351
Start	26136224:26136224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1347G>A
AA Mutation	p.Trp449Ter(p.W449*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript