Colon Cancer: Gene >> CXCR5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000292174
Start	118893629:118893629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.85G>A
AA Mutation	p.Asp29Asn(p.D29N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000292174
Start	118894533:118894533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.989G>A
AA Mutation	p.Arg330His(p.R330H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000292174
Start	118893899:118893899(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.355A>G
AA Mutation	p.Thr119Ala(p.T119A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000292174
Start	118894020:118894020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.476G>A
AA Mutation	p.Arg159His(p.R159H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000292174
Start	118893977:118893977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.433G>A
AA Mutation	p.Val145Met(p.V145M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000292174
Start	118894326:118894326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.782C>T
AA Mutation	p.Ala261Val(p.A261V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000292174
Start	118893983:118893983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.439C>T
AA Mutation	p.Arg147Cys(p.R147C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000292174
Start	118893841:118893841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774062762
CDS Mutation	c.297G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000292174
Start	118894546:118894546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147267963
CDS Mutation	c.1002G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000292174
Start	118894633:118894634(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1092_1093delGA
AA Mutation	p.Asn365CysfsTer46(p.N365Cfs*46)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CXCR5

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000292174
Start	118894199:118894199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373329724
CDS Mutation	c.655C>T
AA Mutation	p.Arg219Ter(p.R219*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript