Colon Cancer: Gene >> ACKR3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000272928
Start	236581379:236581379(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.914T>C
AA Mutation	p.Leu305Pro(p.L305P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000272928
Start	236581230:236581230(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.765C>A
AA Mutation	p.Phe255Leu(p.F255L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000272928
Start	236581423:236581423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371364738
CDS Mutation	c.958C>T
AA Mutation	p.Arg320Cys(p.R320C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000272928
Start	236581216:236581216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201845893
CDS Mutation	c.751C>T
AA Mutation	p.Arg251Trp(p.R251W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000272928
Start	236580947:236580947(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.482G>A
AA Mutation	p.Arg161His(p.R161H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000272928
Start	236581217:236581217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771402831
CDS Mutation	c.752G>A
AA Mutation	p.Arg251Gln(p.R251Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000272928
Start	236580701:236580701(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200095631
CDS Mutation	c.236C>T
AA Mutation	p.Thr79Met(p.T79M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000272928
Start	236580926:236580926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.461G>A
AA Mutation	p.Ser154Asn(p.S154N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000272928
Start	236581339:236581339(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764138712
CDS Mutation	c.874G>A
AA Mutation	p.Ala292Thr(p.A292T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000272928
Start	236581327:236581327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201423512
CDS Mutation	c.862C>T
AA Mutation	p.Arg288Trp(p.R288W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000272928
Start	236580979:236580979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.514G>A
AA Mutation	p.Ala172Thr(p.A172T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000272928
Start	236581306:236581306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.841C>T
AA Mutation	p.His281Tyr(p.H281Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000272928
Start	236580602:236580602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200114828
CDS Mutation	c.137C>T
AA Mutation	p.Thr46Met(p.T46M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000272928
Start	236580950:236580950(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747331262
CDS Mutation	c.485G>A
AA Mutation	p.Arg162His(p.R162H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000272928
Start	236580603:236580603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375172239
CDS Mutation	c.138G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000272928
Start	236580804:236580804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762709549
CDS Mutation	c.339C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ACKR3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000272928
Start	236580805:236580805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763930150
CDS Mutation	c.340G>A
AA Mutation	p.Glu114Lys(p.E114K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000272928
Start	236580947:236580947(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.482G>A
AA Mutation	p.Arg161His(p.R161H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000272928
Start	236581520:236581520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777382973
CDS Mutation	c.1055C>T
AA Mutation	p.Thr352Met(p.T352M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000272928
Start	236580865:236580865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.400T>G
AA Mutation	p.Phe134Val(p.F134V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000272928
Start	236580483:236580483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750658947
CDS Mutation	c.18C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000272928
Start	236580774:236580774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.309T>C
Mutation Classification	Silent
Feature Type	Transcript