Colon Cancer: Gene >> CCR5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000292303
Start	46373638:46373638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781713216
CDS Mutation	c.736C>A
AA Mutation	p.Leu246Ile(p.L246I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000292303
Start	46373042:46373042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.140G>A
AA Mutation	p.Gly47Asp(p.G47D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000292303
Start	46373300:46373300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.398C>T
AA Mutation	p.Ala133Val(p.A133V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000292303
Start	46372987:46372987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs1800939
CDS Mutation	c.85G>A
AA Mutation	p.Ala29Thr(p.A29T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000292303
Start	46373576:46373576(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764278401
CDS Mutation	c.674G>A
AA Mutation	p.Arg225Gln(p.R225Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000292303
Start	46373521:46373521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.619C>G
AA Mutation	p.Leu207Val(p.L207V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000292303
Start	46373522:46373522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.620T>A
AA Mutation	p.Leu207Gln(p.L207Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000292303
Start	46373251:46373251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.349T>G
AA Mutation	p.Phe117Val(p.F117V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000292303
Start	46373712:46373712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.810T>G
AA Mutation	p.Ser270Arg(p.S270R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000292303
Start	46373134:46373134(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.236delT
AA Mutation	p.Phe79SerfsTer26(p.F79Sfs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000292303
Start	46373133:46373134(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.236dupT
AA Mutation	p.Leu80ProfsTer47(p.L80Pfs*47)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CCR5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000292303
Start	46373691:46373691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.789C>A
AA Mutation	p.Phe263Leu(p.F263L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000292303
Start	46373219:46373219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.317G>T
AA Mutation	p.Gly106Val(p.G106V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000292303
Start	46373712:46373712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.810T>G
AA Mutation	p.Ser270Arg(p.S270R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000292303
Start	46373057:46373057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.155T>C
AA Mutation	p.Ile52Thr(p.I52T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000292303
Start	46373575:46373575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146972949
CDS Mutation	c.673C>T
AA Mutation	p.Arg225Ter(p.R225*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript