Colon Cancer: Gene >> MTOR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11130747:11130747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5395G>A
AA Mutation	p.Glu1799Lys(p.E1799K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11124516:11124516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs587777894
CDS Mutation	c.6644C>T
AA Mutation	p.Ser2215Phe(p.S2215F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11238462:11238462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748207893
CDS Mutation	c.1942G>A
AA Mutation	p.Ala648Thr(p.A648T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11213450:11213450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757645678
CDS Mutation	c.3234G>A
AA Mutation	p.Met1078Ile(p.M1078I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11213497:11213497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3187C>T
AA Mutation	p.Leu1063Phe(p.L1063F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11130675:11130675(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5467G>A
AA Mutation	p.Ala1823Thr(p.A1823T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11126643:11126643(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6505C>T
AA Mutation	p.Pro2169Ser(p.P2169S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000361445
Start	11117004:11117004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7016G>T
AA Mutation	p.Arg2339Ile(p.R2339I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11240377:11240377(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749766561
CDS Mutation	c.1712C>T
AA Mutation	p.Thr571Met(p.T571M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11117021:11117021(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6999T>G
AA Mutation	p.Ile2333Met(p.I2333M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11139308:11139308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs587777895
CDS Mutation	c.5126G>A
AA Mutation	p.Arg1709His(p.R1709H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11259252:11259252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.158G>A
AA Mutation	p.Arg53Gln(p.R53Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11144673:11144673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4847G>A
AA Mutation	p.Arg1616His(p.R1616H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11216158:11216158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3107C>A
AA Mutation	p.Thr1036Asn(p.T1036N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11231353:11231353(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2596G>A
AA Mutation	p.Glu866Lys(p.E866K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11129784:11129784(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5668C>T
AA Mutation	p.Arg1890Cys(p.R1890C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11209382:11209382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3731C>A
AA Mutation	p.Ala1244Glu(p.A1244E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11253930:11253930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.749C>T
AA Mutation	p.Ala250Val(p.A250V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11243121:11243121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763879621
CDS Mutation	c.1405G>A
AA Mutation	p.Ala469Thr(p.A469T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11233453:11233453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2366A>T
AA Mutation	p.Asp789Val(p.D789V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11259349:11259349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149221273
CDS Mutation	c.61G>A
AA Mutation	p.Val21Ile(p.V21I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11122122:11122122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6667C>A
AA Mutation	p.Gln2223Lys(p.Q2223K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11237963:11237963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2088G>T
AA Mutation	p.Leu696Phe(p.L696F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11128926:11128926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5740G>T
AA Mutation	p.Gly1914Cys(p.G1914C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11145002:11145002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4730C>T
AA Mutation	p.Ala1577Val(p.A1577V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11213446:11213446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751901845
CDS Mutation	c.3238C>T
AA Mutation	p.Arg1080Cys(p.R1080C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11257151:11257151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.286G>A
AA Mutation	p.Val96Met(p.V96M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11248003:11248003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150146024
CDS Mutation	c.932G>A
AA Mutation	p.Arg311His(p.R311H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11157182:11157182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780930764
CDS Mutation	c.4439G>A
AA Mutation	p.Arg1480His(p.R1480H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11130767:11130767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5375C>T
AA Mutation	p.Ala1792Val(p.A1792V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11112896:11112896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7322G>A
AA Mutation	p.Arg2441Gln(p.R2441Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11238594:11238594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1810C>T
AA Mutation	p.Arg604Cys(p.R604C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11256029:11256029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.668G>A
AA Mutation	p.Arg223His(p.R223H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11228722:11228722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2976G>T
AA Mutation	p.Gln992His(p.Q992H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	35
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11258503:11258503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.253G>A
AA Mutation	p.Gly85Ser(p.G85S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	36
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11204597:11204597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3908G>T
AA Mutation	p.Cys1303Phe(p.C1303F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	37
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11167480:11167480(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4291G>A
AA Mutation	p.Gly1431Arg(p.G1431R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	38
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11127775:11127775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6065T>C
AA Mutation	p.Leu2022Pro(p.L2022P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	39
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11167494:11167494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs35509012
CDS Mutation	c.4277C>T
AA Mutation	p.Pro1426Leu(p.P1426L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	40
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361445
Start	11114399:11114399(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7219C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	41
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361445
Start	11130661:11130661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769197073
CDS Mutation	c.5481C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	42
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361445
Start	11240523:11240523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369221365
CDS Mutation	c.1566C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	43
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361445
Start	11259350:11259350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.60C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	44
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361445
Start	11128037:11128037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6000G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	45
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361445
Start	11243143:11243143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753907829
CDS Mutation	c.1383G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	46
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361445
Start	11126713:11126713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6435C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	47
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361445
Start	11232487:11232487(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2463delT
AA Mutation	p.Phe821LeufsTer34(p.F821Lfs*34)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	48
Mutation Consequence	stop_gained
Transcription ID	ENST00000361445
Start	11233409:11233409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2410G>T
AA Mutation	p.Glu804Ter(p.E804*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	49
Mutation Consequence	stop_gained
Transcription ID	ENST00000361445
Start	11259343:11259343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.67C>T
AA Mutation	p.Gln23Ter(p.Q23*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> MTOR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11128947:11128947(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5719C>T
AA Mutation	p.Leu1907Phe(p.L1907F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361445
Start	11130646:11130646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5496C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000361445
Start	11109305:11109305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7513C>T
AA Mutation	p.Arg2505Ter(p.R2505*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript