Colon Cancer: Gene >> CXCR4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000241393
Start	136115225:136115225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.703C>T
AA Mutation	p.Arg235Cys(p.R235C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000241393
Start	136114943:136114943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.985C>A
AA Mutation	p.Leu329Ile(p.L329I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000241393
Start	136115590:136115590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.338A>G
AA Mutation	p.His113Arg(p.H113R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000241393
Start	136115873:136115873(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.55G>T
AA Mutation	p.Gly19Trp(p.G19W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000241393
Start	136115527:136115527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.401G>A
AA Mutation	p.Arg134His(p.R134H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000241393
Start	136115387:136115387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.541G>A
AA Mutation	p.Asp181Asn(p.D181N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000241393
Start	136115460:136115460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.468C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000241393
Start	136114983:136114983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144110709
CDS Mutation	c.945C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000241393
Start	136114928:136114928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs104893624
CDS Mutation	c.1000C>T
AA Mutation	p.Arg334Ter(p.R334*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CXCR4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000241393
Start	136115614:136115614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.314G>C
AA Mutation	p.Gly105Ala(p.G105A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000241393
Start	136115180:136115180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771851938
CDS Mutation	c.748G>A
AA Mutation	p.Ala250Thr(p.A250T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000241393
Start	136115283:136115283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.645C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000241393
Start	136115875:136115875(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.53delC
AA Mutation	p.Ser18Ter(p.S18*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript