Colon Cancer: Gene >> CD5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000347785
Start	61118328:61118328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138915999
CDS Mutation	c.248G>A
AA Mutation	p.Arg83Gln(p.R83Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000347785
Start	61118223:61118223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.143T>C
AA Mutation	p.Leu48Pro(p.L48P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000347785
Start	61119317:61119317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.547G>T
AA Mutation	p.Gly183Cys(p.G183C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000347785
Start	61125097:61125097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200669351
CDS Mutation	c.1345G>A
AA Mutation	p.Val449Met(p.V449M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000347785
Start	61118212:61118212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.132C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000347785
Start	61125794:61125794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1443C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000347785
Start	61122962:61122962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1155G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000347785
Start	61121669:61121669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200479488
CDS Mutation	c.864C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000347785
Start	61118188:61118188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141935047
CDS Mutation	c.108G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CD5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000347785
Start	61119342:61119342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.572A>G
AA Mutation	p.Asp191Gly(p.D191G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000347785
Start	61125044:61125044(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139956085
CDS Mutation	c.1292G>A
AA Mutation	p.Arg431His(p.R431H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000347785
Start	61119361:61119361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.591G>T
AA Mutation	p.Glu197Asp(p.E197D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript