Colon Cancer: Gene >> MTMR11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000439741
Start	149933913:149933913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782132670
CDS Mutation	c.713G>A
AA Mutation	p.Arg238Gln(p.R238Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000439741
Start	149929743:149929743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1821G>C
AA Mutation	p.Trp607Cys(p.W607C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000439741
Start	149929655:149929655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371578546
CDS Mutation	c.1909C>T
AA Mutation	p.Arg637Cys(p.R637C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000439741
Start	149929905:149929905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1659G>A
AA Mutation	p.Met553Ile(p.M553I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000439741
Start	149934296:149934296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.578T>C
AA Mutation	p.Ile193Thr(p.I193T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000439741
Start	149929623:149929623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1941G>T
AA Mutation	p.Gln647His(p.Q647H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000439741
Start	149935614:149935614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.234C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000439741
Start	149934214:149934214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200559299
CDS Mutation	c.660C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000439741
Start	149929653:149929653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1911C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000439741
Start	149930867:149930867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782787289
CDS Mutation	c.1389T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000439741
Start	149930819:149930819(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1437delC
AA Mutation	p.Trp480GlyfsTer10(p.W480Gfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000439741
Start	149931325:149931325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782759787
CDS Mutation	c.1225C>T
AA Mutation	p.Arg409Ter(p.R409*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000439741
Start	149936604:149936605(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.43dupC
AA Mutation	p.Gln15ProfsTer14(p.Q15Pfs*14)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MTMR11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000439741
Start	149930373:149930373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1639A>G
AA Mutation	p.Arg547Gly(p.R547G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000439741
Start	149929170:149929170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2089G>C
AA Mutation	p.Ala697Pro(p.A697P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000439741
Start	149936604:149936605(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.43dupC
AA Mutation	p.Gln15ProfsTer14(p.Q15Pfs*14)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript