Colon Cancer: Gene >> ALX4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000329255
Start	44275355:44275355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200419726
CDS Mutation	c.770G>A
AA Mutation	p.Arg257His(p.R257H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000329255
Start	44267499:44267499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766411205
CDS Mutation	c.901G>A
AA Mutation	p.Ala301Thr(p.A301T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000329255
Start	44275472:44275472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs104894193
CDS Mutation	c.653G>A
AA Mutation	p.Arg218Gln(p.R218Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000329255
Start	44309875:44309875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372830230
CDS Mutation	c.188G>A
AA Mutation	p.Arg63Gln(p.R63Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000329255
Start	44264877:44264877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1213G>A
AA Mutation	p.Ala405Thr(p.A405T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000329255
Start	44264900:44264900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763248407
CDS Mutation	c.1190G>A
AA Mutation	p.Arg397His(p.R397H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000329255
Start	44309980:44309980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.83G>A
AA Mutation	p.Arg28Gln(p.R28Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329255
Start	44265163:44265163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747416406
CDS Mutation	c.927C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329255
Start	44275381:44275381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.744C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329255
Start	44275558:44275558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.567G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000329255
Start	44265074:44265074(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1016delC
AA Mutation	p.Pro339LeufsTer12(p.P339Lfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000329255
Start	44275622:44275622(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.503delC
AA Mutation	p.Pro168LeufsTer13(p.P168Lfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ALX4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000329255
Start	44267555:44267555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144440589
CDS Mutation	c.845G>A
AA Mutation	p.Arg282Gln(p.R282Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000329255
Start	44264967:44264967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1123C>T
AA Mutation	p.Pro375Ser(p.P375S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000329255
Start	44309857:44309857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.206G>A
AA Mutation	p.Gly69Glu(p.G69E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329255
Start	44309934:44309934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.129C>T
Mutation Classification	Silent
Feature Type	Transcript