Colon Cancer: Gene >> CD96

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000283285
Start	111542280:111542280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140727933
CDS Mutation	c.32A>G
AA Mutation	p.Tyr11Cys(p.Y11C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000283285
Start	111624371:111624371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1336C>T
AA Mutation	p.Pro446Ser(p.P446S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000283285
Start	111638156:111638156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372441714
CDS Mutation	c.1513G>A
AA Mutation	p.Val505Ile(p.V505I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000283285
Start	111600765:111600765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.986G>T
AA Mutation	p.Gly329Val(p.G329V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000283285
Start	111545180:111545180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.196G>T
AA Mutation	p.Asp66Tyr(p.D66Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000283285
Start	111600903:111600903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1124C>A
AA Mutation	p.Thr375Asn(p.T375N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000283285
Start	111649706:111649706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1658G>T
AA Mutation	p.Arg553Ile(p.R553I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000283285
Start	111649801:111649801(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1753C>A
AA Mutation	p.Leu585Ile(p.L585I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000283285
Start	111600908:111600908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1129C>A
AA Mutation	p.Leu377Ile(p.L377I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000283285
Start	111545143:111545143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140137237
CDS Mutation	c.159C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000283285
Start	111577516:111577516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142203509
CDS Mutation	c.558G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000283285
Start	111579104:111579104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.669C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000283285
Start	111542255:111542255(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.12delA
AA Mutation	p.Lys4AsnfsTer40(p.K4Nfs*40)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000283285
Start	111545055:111545055(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.76delA
AA Mutation	p.Thr26GlnfsTer18(p.T26Qfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000283285
Start	111598207:111598207(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.943G>T
AA Mutation	p.Glu315Ter(p.E315*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000283285
Start	111579102:111579103(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.667_668insAGGAAGAA
AA Mutation	p.Val223GlufsTer38(p.V223Efs*38)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CD96

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000283285
Start	111579188:111579188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763928223
CDS Mutation	c.753C>T
Mutation Classification	Silent
Feature Type	Transcript