Colon Cancer: Gene >> HS3ST2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261374
Start	22814660:22814660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.50C>T
AA Mutation	p.Ala17Val(p.A17V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261374
Start	22814690:22814690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.80C>T
AA Mutation	p.Ser27Leu(p.S27L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261374
Start	22814863:22814863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.253G>A
AA Mutation	p.Ala85Thr(p.A85T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261374
Start	22915072:22915072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.614G>T
AA Mutation	p.Arg205Leu(p.R205L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261374
Start	22915086:22915086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.628C>T
AA Mutation	p.Arg210Cys(p.R210C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000261374
Start	22814965:22814965(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.355A>G
AA Mutation	p.Ile119Val(p.I119V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000261374
Start	22915071:22915071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.613C>T
AA Mutation	p.Arg205Trp(p.R205W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261374
Start	22915196:22915196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.738C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261374
Start	22815072:22815072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.462C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261374
Start	22914992:22914992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145496461
CDS Mutation	c.534G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261374
Start	22915106:22915106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771188795
CDS Mutation	c.648G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000261374
Start	22915497:22915497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1039G>T
AA Mutation	p.Glu347Ter(p.E347*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> HS3ST2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261374
Start	22814993:22814993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.383G>T
AA Mutation	p.Arg128Leu(p.R128L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000261374
Start	22915557:22915557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1099G>T
AA Mutation	p.Glu367Ter(p.E367*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000261374
Start	22915497:22915497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1039G>T
AA Mutation	p.Glu347Ter(p.E347*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript