Colon Cancer: Gene >> RPTOR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000306801
Start	80823180:80823180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1093G>A
AA Mutation	p.Val365Ile(p.V365I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000306801
Start	80823189:80823189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1102C>T
AA Mutation	p.Pro368Ser(p.P368S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000306801
Start	80925422:80925422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150835528
CDS Mutation	c.2861C>T
AA Mutation	p.Thr954Met(p.T954M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000306801
Start	80707844:80707844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.352C>T
AA Mutation	p.Arg118Trp(p.R118W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000306801
Start	80925418:80925418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201551267
CDS Mutation	c.2857G>A
AA Mutation	p.Ala953Thr(p.A953T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000306801
Start	80707905:80707905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.413G>A
AA Mutation	p.Arg138His(p.R138H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000306801
Start	80643743:80643743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.281G>A
AA Mutation	p.Gly94Asp(p.G94D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000306801
Start	80940565:80940565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201400170
CDS Mutation	c.2989C>T
AA Mutation	p.Arg997Cys(p.R997C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000306801
Start	80883851:80883851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1721G>A
AA Mutation	p.Arg574His(p.R574H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000306801
Start	80962525:80962525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3757G>C
AA Mutation	p.Val1253Leu(p.V1253L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000306801
Start	80883932:80883932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1802A>G
AA Mutation	p.His601Arg(p.H601R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000306801
Start	80885128:80885128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1963G>A
AA Mutation	p.Gly655Arg(p.G655R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000306801
Start	80945737:80945737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3096C>A
AA Mutation	p.His1032Gln(p.H1032Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000306801
Start	80945739:80945739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3098C>A
AA Mutation	p.Pro1033His(p.P1033H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000306801
Start	80891768:80891768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2032T>G
AA Mutation	p.Phe678Val(p.F678V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000306801
Start	80962538:80962538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3770C>T
AA Mutation	p.Thr1257Met(p.T1257M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000306801
Start	80822212:80822212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.902G>A
AA Mutation	p.Arg301His(p.R301H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000306801
Start	80707941:80707941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.449A>G
AA Mutation	p.Tyr150Cys(p.Y150C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000306801
Start	80925431:80925431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200514795
CDS Mutation	c.2870C>T
AA Mutation	p.Thr957Met(p.T957M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000306801
Start	80925440:80925440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2879G>A
AA Mutation	p.Cys960Tyr(p.C960Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000306801
Start	80961453:80961453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143802144
CDS Mutation	c.3665G>A
AA Mutation	p.Arg1222His(p.R1222H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306801
Start	80893780:80893780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2316C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306801
Start	80908890:80908890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2481G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306801
Start	80957640:80957640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3387G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306801
Start	80883837:80883837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs7210571
CDS Mutation	c.1707G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306801
Start	80945764:80945764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199631709
CDS Mutation	c.3123C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306801
Start	80883894:80883894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146893435
CDS Mutation	c.1764C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306801
Start	80754120:80754120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.765C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	stop_gained
Transcription ID	ENST00000306801
Start	80957702:80957702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3449G>A
AA Mutation	p.Trp1150Ter(p.W1150*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> RPTOR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000306801
Start	80883815:80883815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1685G>T
AA Mutation	p.Cys562Phe(p.C562F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000306801
Start	80892840:80892840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2213C>A
AA Mutation	p.Ser738Tyr(p.S738Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306801
Start	80880465:80880465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146549130
CDS Mutation	c.1560G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306801
Start	80730577:80730577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.525C>T
Mutation Classification	Silent
Feature Type	Transcript