Colon Cancer: Gene >> CD2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369478
Start	116754636:116754636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.67G>T
AA Mutation	p.Val23Phe(p.V23F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369478
Start	116768608:116768608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.881G>T
AA Mutation	p.Ser294Ile(p.S294I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369478
Start	116754735:116754735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.166G>A
AA Mutation	p.Asp56Asn(p.D56N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000369478
Start	116754710:116754710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.141T>G
AA Mutation	p.Ser47Arg(p.S47R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369478
Start	116754911:116754911(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.347delA
AA Mutation	p.Asn116MetfsTer9(p.N116Mfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369478
Start	116754925:116754925(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.361delA
AA Mutation	p.Ile121TyrfsTer4(p.I121Yfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CD2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369478
Start	116754797:116754797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.228G>T
AA Mutation	p.Glu76Asp(p.E76D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369478
Start	116754889:116754889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.320T>C
AA Mutation	p.Val107Ala(p.V107A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript