Colon Cancer: Gene >> ARL6IP6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000326446
Start	152718756:152718756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.132G>C
AA Mutation	p.Glu44Asp(p.E44D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000326446
Start	152719000:152719000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.376G>A
AA Mutation	p.Ala126Thr(p.A126T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000326446
Start	152735023:152735023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.484A>G
AA Mutation	p.Thr162Ala(p.T162A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000326446
Start	152718949:152718949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.325C>A
AA Mutation	p.Leu109Ile(p.L109I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000326446
Start	152719026:152719026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.400+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> ARL6IP6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000326446
Start	152718970:152718970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.346C>T
AA Mutation	p.Leu116Phe(p.L116F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript