Colon Cancer: Gene >> MTTP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265517
Start	99583428:99583428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.304T>G
AA Mutation	p.Phe102Val(p.F102V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265517
Start	99621120:99621120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2402T>G
AA Mutation	p.Leu801Arg(p.L801R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265517
Start	99600720:99600720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1223T>G
AA Mutation	p.Leu408Arg(p.L408R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265517
Start	99606765:99606765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1362G>T
AA Mutation	p.Lys454Asn(p.K454N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265517
Start	99619070:99619070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2314C>T
AA Mutation	p.Arg772Cys(p.R772C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265517
Start	99611192:99611192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749466528
CDS Mutation	c.1819C>T
AA Mutation	p.Arg607Cys(p.R607C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000265517
Start	99582016:99582016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201464944
CDS Mutation	c.173G>A
AA Mutation	p.Arg58His(p.R58H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000265517
Start	99622785:99622785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2622C>A
AA Mutation	p.Asn874Lys(p.N874K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000265517
Start	99622682:99622682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2519T>C
AA Mutation	p.Phe840Ser(p.F840S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000265517
Start	99611445:99611445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs113337987
CDS Mutation	c.1981G>A
AA Mutation	p.Gly661Ser(p.G661S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000265517
Start	99589695:99589695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.446A>G
AA Mutation	p.Lys149Arg(p.K149R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000265517
Start	99601667:99601667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1297G>A
AA Mutation	p.Gly433Arg(p.G433R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000265517
Start	99611346:99611346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1882G>A
AA Mutation	p.Ala628Thr(p.A628T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000265517
Start	99611341:99611341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs568076672
CDS Mutation	c.1877G>A
AA Mutation	p.Arg626His(p.R626H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000265517
Start	99612959:99612959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765550172
CDS Mutation	c.2036C>A
AA Mutation	p.Pro679His(p.P679H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000265517
Start	99606868:99606868(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1465C>A
AA Mutation	p.Leu489Ile(p.L489I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000265517
Start	99582060:99582060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.217G>A
AA Mutation	p.Asp73Asn(p.D73N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265517
Start	99608825:99608825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773522041
CDS Mutation	c.1617G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265517
Start	99613047:99613047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768562163
CDS Mutation	c.2124C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265517
Start	99613131:99613131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780110509
CDS Mutation	c.2208T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265517
Start	99574929:99574929(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.24delT
AA Mutation	p.Leu9SerfsTer20(p.L9Sfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265517
Start	99612966:99612966(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2047delG
AA Mutation	p.Glu683ArgfsTer31(p.E683Rfs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000265517
Start	99622678:99622678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2515C>T
AA Mutation	p.Gln839Ter(p.Q839*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	stop_gained
Transcription ID	ENST00000265517
Start	99608904:99608904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1696G>T
AA Mutation	p.Glu566Ter(p.E566*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000265517
Start	99611241:99611241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764189338
CDS Mutation	c.1867+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> MTTP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265517
Start	99611154:99611154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201863511
CDS Mutation	c.1781G>A
AA Mutation	p.Arg594His(p.R594H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265517
Start	99591271:99591271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.538G>A
AA Mutation	p.Ala180Thr(p.A180T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265517
Start	99597177:99597177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1020G>T
AA Mutation	p.Lys340Asn(p.K340N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265517
Start	99612949:99612949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760037070
CDS Mutation	c.2026G>A
AA Mutation	p.Ala676Thr(p.A676T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265517
Start	99608959:99608959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199664737
CDS Mutation	c.1751G>A
AA Mutation	p.Arg584His(p.R584H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265517
Start	99608876:99608876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751421159
CDS Mutation	c.1668C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265517
Start	99591243:99591243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.510C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265517
Start	99581927:99581927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.84A>G
Mutation Classification	Silent
Feature Type	Transcript