Colon Cancer: Gene >> ARSF

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359361
Start	3072078:3072078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139923989
CDS Mutation	c.64G>A
AA Mutation	p.Ala22Thr(p.A22T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359361
Start	3084378:3084378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs182964743
CDS Mutation	c.542C>T
AA Mutation	p.Thr181Met(p.T181M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359361
Start	3110132:3110132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1270A>G
AA Mutation	p.Ile424Val(p.I424V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000359361
Start	3103842:3103842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141853880
CDS Mutation	c.1183C>T
AA Mutation	p.Arg395Trp(p.R395W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000359361
Start	3076636:3076636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.250G>A
AA Mutation	p.Ala84Thr(p.A84T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359361
Start	3112184:3112184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1401T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359361
Start	3103799:3103799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138210846
CDS Mutation	c.1140C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359361
Start	3110227:3110227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144086355
CDS Mutation	c.1365C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359361
Start	3112382:3112382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1599G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359361
Start	3084550:3084550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764936345
CDS Mutation	c.714G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000359361
Start	3084620:3084620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200082842
CDS Mutation	c.784C>T
AA Mutation	p.Arg262Ter(p.R262*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359361
Start	3103875:3103876(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1220dupT
AA Mutation	p.Leu407PhefsTer19(p.L407Ffs*19)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ARSF

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359361
Start	3101107:3101107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746645956
CDS Mutation	c.988G>A
AA Mutation	p.Asp330Asn(p.D330N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359361
Start	3112289:3112289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1506C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000359361
Start	3112269:3112269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1486G>T
AA Mutation	p.Glu496Ter(p.E496*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript