Colon Cancer: Gene >> B3GAT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000312527
Start	134384032:134384032(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.269C>T
AA Mutation	p.Thr90Met(p.T90M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000312527
Start	134382825:134382825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368413334
CDS Mutation	c.803G>A
AA Mutation	p.Arg268Gln(p.R268Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000312527
Start	134383817:134383817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746356457
CDS Mutation	c.484C>T
AA Mutation	p.Arg162Cys(p.R162C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000312527
Start	134382787:134382787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.841G>T
AA Mutation	p.Gly281Cys(p.G281C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000312527
Start	134384099:134384099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.202C>T
AA Mutation	p.Arg68Cys(p.R68C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000312527
Start	134382840:134382840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750780574
CDS Mutation	c.788G>A
AA Mutation	p.Arg263Gln(p.R263Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000312527
Start	134387572:134387572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769059991
CDS Mutation	c.88G>A
AA Mutation	p.Ala30Thr(p.A30T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000312527
Start	134387620:134387620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376707624
CDS Mutation	c.40G>A
AA Mutation	p.Val14Met(p.V14M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312527
Start	134384127:134384127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755439844
CDS Mutation	c.174G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312527
Start	134383716:134383716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763700916
CDS Mutation	c.585C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312527
Start	134383779:134383779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.522G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312527
Start	134383686:134383686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.615C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> B3GAT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000312527
Start	134381997:134381997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.946A>G
AA Mutation	p.Lys316Glu(p.K316E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000312527
Start	134382910:134382910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.718G>A
AA Mutation	p.Gly240Ser(p.G240S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript