Colon Cancer: Gene >> ARL11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000282026
Start	49630637:49630637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143660006
CDS Mutation	c.190G>A
AA Mutation	p.Val64Ile(p.V64I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000282026
Start	49630790:49630790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.343G>A
AA Mutation	p.Val115Ile(p.V115I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000282026
Start	49630527:49630527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.80C>T
AA Mutation	p.Thr27Met(p.T27M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000282026
Start	49630700:49630700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374531869
CDS Mutation	c.253G>A
AA Mutation	p.Val85Met(p.V85M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000282026
Start	49630648:49630648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.201G>T
AA Mutation	p.Gln67His(p.Q67H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282026
Start	49630645:49630645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.198G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282026
Start	49630663:49630663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.216C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000282026
Start	49630640:49630640(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.198delG
AA Mutation	p.Gln67ArgfsTer41(p.Q67Rfs*41)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000282026
Start	49630639:49630640(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.198dupG
AA Mutation	p.Gln67AlafsTer27(p.Q67Afs*27)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ARL11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000282026
Start	49630479:49630479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs566163670
CDS Mutation	c.32C>T
AA Mutation	p.Ala11Val(p.A11V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript