Colon Cancer: Gene >> ALCAM

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000306107
Start	105545269:105545269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1038T>G
AA Mutation	p.Ile346Met(p.I346M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000306107
Start	105571915:105571915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1728A>C
AA Mutation	p.Glu576Asp(p.E576D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000306107
Start	105547448:105547448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1299A>G
AA Mutation	p.Ile433Met(p.I433M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000306107
Start	105545331:105545331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1100T>C
AA Mutation	p.Met367Thr(p.M367T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306107
Start	105533674:105533674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.531A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000306107
Start	105532060:105532060(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.458delA
AA Mutation	p.Lys153SerfsTer34(p.K153Sfs*34)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000306107
Start	105520167:105520167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.174T>G
AA Mutation	p.Tyr58Ter(p.Y58*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000306107
Start	105547164:105547164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1120C>T
AA Mutation	p.Arg374Ter(p.R374*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000306107
Start	105552521:105552522(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1602dupT
AA Mutation	p.Gly535TrpfsTer33(p.G535Wfs*33)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ALCAM

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000306107
Start	105520109:105520109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.116T>A
AA Mutation	p.Ile39Asn(p.I39N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript