Colon Cancer: Gene >> MTMR3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000401950
Start	29991554:29991554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.344A>G
AA Mutation	p.Asn115Ser(p.N115S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000401950
Start	30013407:30013407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1369G>A
AA Mutation	p.Ala457Thr(p.A457T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000401950
Start	29991559:29991559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755138094
CDS Mutation	c.349G>A
AA Mutation	p.Ala117Thr(p.A117T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000401950
Start	30020534:30020534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755680177
CDS Mutation	c.2875G>A
AA Mutation	p.Ala959Thr(p.A959T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000401950
Start	30020790:30020790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3131C>T
AA Mutation	p.Thr1044Ile(p.T1044I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000401950
Start	30020574:30020574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141681560
CDS Mutation	c.2915G>A
AA Mutation	p.Arg972His(p.R972H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000401950
Start	29998779:29998779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.479G>T
AA Mutation	p.Arg160Met(p.R160M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000401950
Start	30019942:30019942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2283C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000401950
Start	30016572:30016572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1548C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000401950
Start	30019783:30019783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2124C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000401950
Start	30018059:30018059(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1813delC
AA Mutation	p.Leu605Ter(p.L605*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000401950
Start	30008002:30008002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.979C>T
AA Mutation	p.Arg327Ter(p.R327*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000401950
Start	30013433:30013434(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1395_1396insATTTG
AA Mutation	p.Ser466IlefsTer6(p.S466Ifs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MTMR3

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000401950
Start	29978937:29978937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.95T>A
AA Mutation	p.Val32Asp(p.V32D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000401950
Start	30020042:30020042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2383C>G
AA Mutation	p.Gln795Glu(p.Q795E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000401950
Start	29978489:29978489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.51C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000401950
Start	29991671:29991671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.460+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript