Colon Cancer: Gene >> ACKR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000273145
Start	42865025:42865025(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.523G>A
AA Mutation	p.Val175Ile(p.V175I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000273145
Start	42864720:42864720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.218G>A
AA Mutation	p.Arg73His(p.R73H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000273145
Start	42865242:42865242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.740G>A
AA Mutation	p.Arg247Gln(p.R247Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000273145
Start	42865103:42865103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368758367
CDS Mutation	c.601G>A
AA Mutation	p.Gly201Arg(p.G201R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000273145
Start	42864522:42864522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780739221
CDS Mutation	c.20C>T
AA Mutation	p.Pro7Leu(p.P7L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273145
Start	42865489:42865489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.987C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273145
Start	42865102:42865102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375376109
CDS Mutation	c.600C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273145
Start	42864949:42864949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150917727
CDS Mutation	c.447T>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ACKR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000273145
Start	42865586:42865586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1084A>G
AA Mutation	p.Met362Val(p.M362V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000273145
Start	42864975:42864975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764776544
CDS Mutation	c.473G>A
AA Mutation	p.Arg158Gln(p.R158Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000273145
Start	42865252:42865252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.750A>C
AA Mutation	p.Lys250Asn(p.K250N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000273145
Start	42864748:42864748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.246G>T
AA Mutation	p.Glu82Asp(p.E82D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript