Colon Cancer: Gene >> CD14

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302014
Start	140631920:140631920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748409113
CDS Mutation	c.1064C>T
AA Mutation	p.Ser355Leu(p.S355L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000302014
Start	140632140:140632140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.844A>C
AA Mutation	p.Asn282His(p.N282H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000302014
Start	140632683:140632683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.301G>C
AA Mutation	p.Val101Leu(p.V101L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000302014
Start	140631876:140631876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1108G>A
AA Mutation	p.Gly370Arg(p.G370R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000302014
Start	140632345:140632345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.639G>A
AA Mutation	p.Met213Ile(p.M213I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000302014
Start	140632545:140632545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.439T>G
AA Mutation	p.Leu147Val(p.L147V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	protein_altering_variant
Transcription ID	ENST00000302014
Start	140632220:140632221(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.763_764insTTATCC
AA Mutation	p.Asp255delinsValIleHis(p.D255delinsVIH)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CD14

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302014
Start	140632328:140632328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.656A>G
AA Mutation	p.His219Arg(p.H219R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript