Colon Cancer: Gene >> GUSB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000304895
Start	65964341:65964341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1771G>A
AA Mutation	p.Asp591Asn(p.D591N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000304895
Start	65980315:65980315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.305A>G
AA Mutation	p.Glu102Gly(p.E102G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000304895
Start	65967780:65967780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1604C>T
AA Mutation	p.Pro535Leu(p.P535L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000304895
Start	65979470:65979470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.653T>C
AA Mutation	p.Val218Ala(p.V218A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000304895
Start	65967810:65967810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1574T>G
AA Mutation	p.Phe525Cys(p.F525C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304895
Start	65979897:65979897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141441283
CDS Mutation	c.411C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304895
Start	65982154:65982154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.30G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000304895
Start	65980292:65980292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.328C>T
AA Mutation	p.Arg110Ter(p.R110*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> GUSB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000304895
Start	65976119:65976119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.808G>A
AA Mutation	p.Val270Met(p.V270M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000304895
Start	65974539:65974539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1231G>A
AA Mutation	p.Gly411Ser(p.G411S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304895
Start	65979813:65979813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.495G>T
Mutation Classification	Silent
Feature Type	Transcript