Colon Cancer: Gene >> FAS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000355740
Start	89008894:89008894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773565107
CDS Mutation	c.340G>A
AA Mutation	p.Glu114Lys(p.E114K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000355740
Start	89008916:89008916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.362G>A
AA Mutation	p.Arg121Gln(p.R121Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000355740
Start	89014239:89014239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.797A>T
AA Mutation	p.Asn266Ile(p.N266I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000355740
Start	89010789:89010789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.542T>C
AA Mutation	p.Leu181Pro(p.L181P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000355740
Start	89008951:89008951(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.403delT
AA Mutation	p.Cys135ValfsTer52(p.C135Vfs*52)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000355740
Start	89014336:89014337(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.900dupA
AA Mutation	p.Ala301SerfsTer20(p.A301Sfs*20)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000355740
Start	89008950:89008951(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.403dupT
AA Mutation	p.Cys135LeufsTer2(p.C135Lfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	start_lost
Transcription ID	ENST00000355740
Start	88990879:88990879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3G>A
AA Mutation	p.Met1?(p.M1?)
Mutation Classification	Translation_Start_Site
Feature Type	Transcript

Rectum Cancer: Gene >> FAS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000355740
Start	89014367:89014367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.925A>C
AA Mutation	p.Lys309Gln(p.K309Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000355740
Start	89014191:89014191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.749G>A
AA Mutation	p.Arg250Gln(p.R250Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355740
Start	89007815:89007815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.312T>C
Mutation Classification	Silent
Feature Type	Transcript