Colon Cancer: Gene >> RMI1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000325875
Start	84001484:84001484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.498A>C
AA Mutation	p.Lys166Asn(p.K166N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000325875
Start	84001059:84001059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.73A>G
AA Mutation	p.Met25Val(p.M25V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000325875
Start	84001924:84001924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.938A>C
AA Mutation	p.Asp313Ala(p.D313A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000325875
Start	84002411:84002411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1425G>T
AA Mutation	p.Glu475Asp(p.E475D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000325875
Start	84001462:84001462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.476G>T
AA Mutation	p.Ser159Ile(p.S159I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000325875
Start	84001114:84001114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.128T>C
AA Mutation	p.Leu43Ser(p.L43S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000325875
Start	84001591:84001591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.605C>T
AA Mutation	p.Ala202Val(p.A202V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000325875
Start	84002026:84002026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748426652
CDS Mutation	c.1040G>A
AA Mutation	p.Arg347Gln(p.R347Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000325875
Start	84002243:84002243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769434409
CDS Mutation	c.1257G>T
AA Mutation	p.Lys419Asn(p.K419N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000325875
Start	84002748:84002748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1762T>G
AA Mutation	p.Leu588Val(p.L588V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000325875
Start	84002263:84002263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1277A>T
AA Mutation	p.Lys426Ile(p.K426I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325875
Start	84002243:84002243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1257G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325875
Start	84002432:84002432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1446T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000325875
Start	84001095:84001095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.109G>T
AA Mutation	p.Glu37Ter(p.E37*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> RMI1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000325875
Start	84002788:84002788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1802C>A
AA Mutation	p.Ser601Tyr(p.S601Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000325875
Start	84001761:84001761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138543013
CDS Mutation	c.775G>A
AA Mutation	p.Ala259Thr(p.A259T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000325875
Start	84002243:84002243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769434409
CDS Mutation	c.1257G>T
AA Mutation	p.Lys419Asn(p.K419N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000325875
Start	84002860:84002860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1874A>C
AA Mutation	p.Lys625Thr(p.K625T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000325875
Start	84002745:84002745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1759G>C
AA Mutation	p.Asp587His(p.D587H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325875
Start	84002834:84002834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1848T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325875
Start	84001604:84001604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.618A>G
Mutation Classification	Silent
Feature Type	Transcript