Colon Cancer: Gene >> HS6ST1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000259241
Start	128268533:128268533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.865G>A
AA Mutation	p.Ala289Thr(p.A289T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000259241
Start	128268347:128268347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1051G>A
AA Mutation	p.Ala351Thr(p.A351T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000259241
Start	128268809:128268809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.589C>T
AA Mutation	p.His197Tyr(p.H197Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000259241
Start	128268644:128268644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773632691
CDS Mutation	c.754C>T
AA Mutation	p.Arg252Cys(p.R252C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000259241
Start	128268253:128268253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1145G>T
AA Mutation	p.Arg382Leu(p.R382L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000259241
Start	128268540:128268540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.858G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000259241
Start	128268423:128268423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs188637045
CDS Mutation	c.975C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> HS6ST1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000259241
Start	128268706:128268706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370343793
CDS Mutation	c.692C>T
AA Mutation	p.Ser231Leu(p.S231L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000259241
Start	128268778:128268778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs267598868
CDS Mutation	c.620C>T
AA Mutation	p.Ser207Leu(p.S207L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000259241
Start	128268777:128268777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs1055575
CDS Mutation	c.621G>A
Mutation Classification	Silent
Feature Type	Transcript