Colon Cancer: Gene >> CD244

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368033
Start	160841712:160841712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.251G>A
AA Mutation	p.Ser84Asn(p.S84N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368033
Start	160839005:160839005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs572370510
CDS Mutation	c.715G>A
AA Mutation	p.Ala239Thr(p.A239T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368033
Start	160841387:160841387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.493G>A
AA Mutation	p.Val165Met(p.V165M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000368033
Start	160838458:160838458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.842G>T
AA Mutation	p.Arg281Ile(p.R281I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000368033
Start	160841495:160841495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.385C>A
AA Mutation	p.Leu129Met(p.L129M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368033
Start	160831356:160831356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1104T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CD244

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368033
Start	160841608:160841608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.355G>A
AA Mutation	p.Ala119Thr(p.A119T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368033
Start	160841442:160841442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.438G>A
Mutation Classification	Silent
Feature Type	Transcript