Colon Cancer: Gene >> B4GALNT3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000266383
Start	544885:544885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756076751
CDS Mutation	c.451C>T
AA Mutation	p.Arg151Cys(p.R151C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000266383
Start	558083:558083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs539329065
CDS Mutation	c.2602G>A
AA Mutation	p.Val868Met(p.V868M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000266383
Start	553883:553883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1960G>A
AA Mutation	p.Asp654Asn(p.D654N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000266383
Start	544886:544886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201901859
CDS Mutation	c.452G>A
AA Mutation	p.Arg151His(p.R151H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266383
Start	556856:556856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150365241
CDS Mutation	c.2370C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266383
Start	556607:556607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2121T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266383
Start	553711:553711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1788C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266383
Start	549791:549791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.876T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266383
Start	553852:553852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376820641
CDS Mutation	c.1929C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266383
Start	460520:460520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.144G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> B4GALNT3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000266383
Start	558514:558514(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2614C>G
AA Mutation	p.His872Asp(p.H872D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266383
Start	536271:536271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.327C>T
Mutation Classification	Silent
Feature Type	Transcript