Colon Cancer: Gene >> MNT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000174618
Start	2387607:2387607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146563186
CDS Mutation	c.1043C>T
AA Mutation	p.Ala348Val(p.A348V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000174618
Start	2395352:2395352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.176G>C
AA Mutation	p.Arg59Pro(p.R59P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000174618
Start	2387248:2387248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769757715
CDS Mutation	c.1402G>A
AA Mutation	p.Ala468Thr(p.A468T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000174618
Start	2387050:2387050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1600G>T
AA Mutation	p.Gly534Cys(p.G534C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000174618
Start	2395153:2395153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377109755
CDS Mutation	c.375C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000174618
Start	2395075:2395075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372877661
CDS Mutation	c.453G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000174618
Start	2387075:2387075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368726975
CDS Mutation	c.1575G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000174618
Start	2387645:2387645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1005T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000174618
Start	2395084:2395084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.444C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000174618
Start	2394963:2394963(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.565delC
AA Mutation	p.Gln189SerfsTer11(p.Q189Sfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000174618
Start	2387343:2387343(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1307delG
AA Mutation	p.Gly436ValfsTer20(p.G436Vfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000174618
Start	2387076:2387076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1574C>A
AA Mutation	p.Ser525Ter(p.S525*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000174618
Start	2394874:2394874(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.653+1delG
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> MNT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000174618
Start	2387089:2387089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750625027
CDS Mutation	c.1561G>A
AA Mutation	p.Ala521Thr(p.A521T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000174618
Start	2386972:2386972(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1678C>T
AA Mutation	p.Gln560Ter(p.Q560*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript