Colon Cancer: Gene >> CCR7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000246657
Start	40555448:40555448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.431T>C
AA Mutation	p.Met144Thr(p.M144T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000246657
Start	40555080:40555080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764245161
CDS Mutation	c.799G>A
AA Mutation	p.Ala267Thr(p.A267T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000246657
Start	40554821:40554821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200794532
CDS Mutation	c.1058G>A
AA Mutation	p.Arg353Gln(p.R353Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000246657
Start	40555343:40555343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.536G>T
AA Mutation	p.Cys179Phe(p.C179F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000246657
Start	40554791:40554791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374797000
CDS Mutation	c.1088G>A
AA Mutation	p.Arg363His(p.R363H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000246657
Start	40554953:40554953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.926A>G
AA Mutation	p.Asp309Gly(p.D309G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000246657
Start	40555719:40555719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.160C>T
AA Mutation	p.Arg54Trp(p.R54W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246657
Start	40555009:40555009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.870C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246657
Start	40555669:40555669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367712364
CDS Mutation	c.210C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246657
Start	40558926:40558926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs193282140
CDS Mutation	c.27C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246657
Start	40554955:40554955(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs116263918
CDS Mutation	c.924C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CCR7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000246657
Start	40555719:40555719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.160C>T
AA Mutation	p.Arg54Trp(p.R54W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000246657
Start	40555742:40555742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.137C>A
AA Mutation	p.Ser46Tyr(p.S46Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript