Colon Cancer: Gene >> RHOBTB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000337910
Start	60875012:60875012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1757C>T
AA Mutation	p.Ala586Val(p.A586V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000337910
Start	60911485:60911485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.58G>A
AA Mutation	p.Val20Met(p.V20M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000337910
Start	60875033:60875033(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1736C>T
AA Mutation	p.Ala579Val(p.A579V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000337910
Start	60911458:60911458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777754426
CDS Mutation	c.85C>T
AA Mutation	p.Arg29Cys(p.R29C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000337910
Start	60888976:60888976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.692C>T
AA Mutation	p.Ala231Val(p.A231V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000337910
Start	60871579:60871579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143799442
CDS Mutation	c.1994G>A
AA Mutation	p.Arg665His(p.R665H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000337910
Start	60888491:60888491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762801403
CDS Mutation	c.1177C>T
AA Mutation	p.Arg393Trp(p.R393W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000337910
Start	60888720:60888720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.948G>C
AA Mutation	p.Gln316His(p.Q316H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000337910
Start	60892958:60892958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.334C>T
AA Mutation	p.Pro112Ser(p.P112S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000337910
Start	60872212:60872212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746517061
CDS Mutation	c.1894C>T
AA Mutation	p.Arg632Cys(p.R632C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000337910
Start	60888823:60888823(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201980179
CDS Mutation	c.845G>A
AA Mutation	p.Arg282Gln(p.R282Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000337910
Start	60871624:60871624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1949G>A
AA Mutation	p.Arg650His(p.R650H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000337910
Start	60872266:60872266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138580713
CDS Mutation	c.1840G>A
AA Mutation	p.Ala614Thr(p.A614T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000337910
Start	60889044:60889044(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772792443
CDS Mutation	c.624G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000337910
Start	60911531:60911531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.12C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000337910
Start	60911459:60911459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749006790
CDS Mutation	c.84G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000337910
Start	60888219:60888219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761872807
CDS Mutation	c.1449G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000337910
Start	60888585:60888585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766201965
CDS Mutation	c.1083C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000337910
Start	60872222:60872222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1884C>A
AA Mutation	p.Cys628Ter(p.C628*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> RHOBTB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000337910
Start	60878041:60878041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1593A>G
AA Mutation	p.Ile531Met(p.I531M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000337910
Start	60875005:60875005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs556718498
CDS Mutation	c.1764G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000337910
Start	60886145:60886145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752021075
CDS Mutation	c.1542C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000337910
Start	60888980:60888980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.688C>T
AA Mutation	p.Gln230Ter(p.Q230*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000337910
Start	60889069:60889070(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.597_598dupGT
AA Mutation	p.Phe200CysfsTer10(p.F200Cfs*10)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript