Colon Cancer: Gene >> CCR3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357422
Start	46266084:46266084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200478041
CDS Mutation	c.926G>A
AA Mutation	p.Arg309Gln(p.R309Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000357422
Start	46266063:46266063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.905C>A
AA Mutation	p.Ala302Asp(p.A302D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000357422
Start	46266008:46266008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.850C>A
AA Mutation	p.Leu284Met(p.L284M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000357422
Start	46265400:46265400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.242T>C
AA Mutation	p.Leu81Pro(p.L81P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000357422
Start	46265283:46265283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.125C>A
AA Mutation	p.Ser42Tyr(p.S42Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000357422
Start	46265256:46265256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.98T>C
AA Mutation	p.Met33Thr(p.M33T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000357422
Start	46265471:46265471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.313A>G
AA Mutation	p.Met105Val(p.M105V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000357422
Start	46266072:46266072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.914G>T
AA Mutation	p.Gly305Val(p.G305V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357422
Start	46265668:46265668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.510C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000357422
Start	46265457:46265457(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.303delT
AA Mutation	p.Phe101LeufsTer24(p.F101Lfs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000357422
Start	46265852:46265852(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs775866199
CDS Mutation	c.701delA
AA Mutation	p.Lys234SerfsTer52(p.K234Sfs*52)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000357422
Start	46265354:46265354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201795127
CDS Mutation	c.196C>T
AA Mutation	p.Arg66Ter(p.R66*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CCR3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357422
Start	46265874:46265874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142051640
CDS Mutation	c.716G>A
AA Mutation	p.Arg239Gln(p.R239Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000357422
Start	46265586:46265586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs56177184
CDS Mutation	c.428G>A
AA Mutation	p.Arg143Gln(p.R143Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000357422
Start	46265516:46265516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.358G>A
AA Mutation	p.Glu120Lys(p.E120K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357422
Start	46265875:46265875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.717G>A
Mutation Classification	Silent
Feature Type	Transcript