Colon Cancer: Gene >> SMOX

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000305958
Start	4177500:4177500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375716040
CDS Mutation	c.358G>A
AA Mutation	p.Val120Met(p.V120M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000305958
Start	4175143:4175143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.88A>T
AA Mutation	p.Ile30Phe(p.I30F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000305958
Start	4181903:4181903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779907818
CDS Mutation	c.536G>A
AA Mutation	p.Arg179His(p.R179H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000305958
Start	4175155:4175155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.100T>A
AA Mutation	p.Leu34Met(p.L34M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000305958
Start	4187291:4187291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370133256
CDS Mutation	c.1552G>A
AA Mutation	p.Gly518Ser(p.G518S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305958
Start	4182739:4182739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139432235
CDS Mutation	c.1260C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305958
Start	4182631:4182631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1152A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305958
Start	4182343:4182343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs562488874
CDS Mutation	c.864C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000305958
Start	4182381:4182381(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.908delG
AA Mutation	p.Gly303AlafsTer20(p.G303Afs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000305958
Start	4181871:4181871(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.508delG
AA Mutation	p.Val170CysfsTer24(p.V170Cfs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000305958
Start	4187388:4187388(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1649delT
AA Mutation	p.Leu550ProfsTer13(p.L550Pfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000305958
Start	4182380:4182381(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs746816975
CDS Mutation	c.908dupG
AA Mutation	p.Arg304GlnfsTer4(p.R304Qfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SMOX

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000305958
Start	4181836:4181836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760977109
CDS Mutation	c.469G>A
AA Mutation	p.Asp157Asn(p.D157N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript