Colon Cancer: Gene >> CHRNB1

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000306071
Start	7455454:7455454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1215T>A
AA Mutation	p.Asn405Lys(p.N405K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000306071
Start	7446884:7446884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.295G>A
AA Mutation	p.Asp99Asn(p.D99N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000306071
Start	7445307:7445307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.96G>T
AA Mutation	p.Glu32Asp(p.E32D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000306071
Start	7447107:7447107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.418C>T
AA Mutation	p.Arg140Cys(p.R140C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000306071
Start	7455814:7455814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1238C>T
AA Mutation	p.Ala413Val(p.A413V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000306071
Start	7455859:7455859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1283C>T
AA Mutation	p.Ala428Val(p.A428V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306071
Start	7448775:7448775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.807G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306071
Start	7445331:7445331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.120C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306071
Start	7446877:7446877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.288C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306071
Start	7455334:7455334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1095C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000306071
Start	7447116:7447116(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.431delC
AA Mutation	p.Pro144ArgfsTer74(p.P144Rfs*74)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000306071
Start	7446084:7446084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.214G>T
AA Mutation	p.Glu72Ter(p.E72*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000306071
Start	7454497:7454498(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1021_1022insT
AA Mutation	p.Gln341LeufsTer49(p.Q341Lfs*49)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CHRNB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000306071
Start	7454367:7454367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.891A>C
AA Mutation	p.Lys297Asn(p.K297N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript