Colon Cancer: Gene >> RIN2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000255006
Start	19974995:19974995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1117C>T
AA Mutation	p.Arg373Trp(p.R373W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000255006
Start	19970891:19970891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs531782187
CDS Mutation	c.737C>T
AA Mutation	p.Ser246Leu(p.S246L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000255006
Start	19996699:19996699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs189523512
CDS Mutation	c.2368G>A
AA Mutation	p.Ala790Thr(p.A790T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000255006
Start	19992242:19992242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2290G>C
AA Mutation	p.Asp764His(p.D764H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000255006
Start	19974746:19974746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.868C>T
AA Mutation	p.Arg290Cys(p.R290C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000255006
Start	19975708:19975708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1830G>T
AA Mutation	p.Met610Ile(p.M610I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000255006
Start	19935160:19935160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.266T>C
AA Mutation	p.Val89Ala(p.V89A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000255006
Start	19974687:19974687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.809C>T
AA Mutation	p.Pro270Leu(p.P270L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000255006
Start	19992271:19992271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2319C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000255006
Start	19974916:19974916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375796105
CDS Mutation	c.1038C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000255006
Start	19975663:19975663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1785C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000255006
Start	19996749:19996749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367964989
CDS Mutation	c.2418G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000255006
Start	19935149:19935149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.255G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000255006
Start	19975594:19975594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1716G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000255006
Start	19974942:19974942(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1070delC
AA Mutation	p.Pro357HisfsTer39(p.P357Hfs*39)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000255006
Start	19975750:19975750(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1878delC
AA Mutation	p.Ile627SerfsTer4(p.I627Sfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000255006
Start	19975749:19975750(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs759390822
CDS Mutation	c.1878dupC
AA Mutation	p.Ile627HisfsTer7(p.I627Hfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000255006
Start	20000731:20000732(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2635dupG
AA Mutation	p.Asp879GlyfsTer3(p.D879Gfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000255006
Start	19975749:19975750(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1877_1878dupCC
AA Mutation	p.Ile627ProfsTer5(p.I627Pfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> RIN2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000255006
Start	19996725:19996725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2394G>T
AA Mutation	p.Lys798Asn(p.K798N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000255006
Start	19996749:19996749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367964989
CDS Mutation	c.2418G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000255006
Start	19975105:19975105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1227G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000255006
Start	19996843:19996843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2511+1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript