Colon Cancer: Gene >> B4GALNT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000300404
Start	49133125:49133125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.100G>A
AA Mutation	p.Gly34Arg(p.G34R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000300404
Start	49160609:49160609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.914C>A
AA Mutation	p.Pro305His(p.P305H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000300404
Start	49168837:49168837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1432G>A
AA Mutation	p.Ala478Thr(p.A478T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000300404
Start	49169598:49169598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1571C>A
AA Mutation	p.Ser524Tyr(p.S524Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000300404
Start	49169670:49169670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375974245
CDS Mutation	c.1643G>A
AA Mutation	p.Arg548Gln(p.R548Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300404
Start	49164194:49164194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs570206637
CDS Mutation	c.1053C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300404
Start	49164140:49164140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.999C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000300404
Start	49168768:49168768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1363G>T
AA Mutation	p.Gly455Ter(p.G455*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> B4GALNT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000300404
Start	49164186:49164186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1045G>T
AA Mutation	p.Asp349Tyr(p.D349Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000300404
Start	49168740:49168740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1335G>T
AA Mutation	p.Glu445Asp(p.E445D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000300404
Start	49168859:49168859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1454G>T
AA Mutation	p.Arg485Ile(p.R485I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300404
Start	49141436:49141436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146112027
CDS Mutation	c.384C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300404
Start	49168803:49168803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776214189
CDS Mutation	c.1398C>T
Mutation Classification	Silent
Feature Type	Transcript