Colon Cancer: Gene >> OAS2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000342315
Start	112995448:112995448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.601C>A
AA Mutation	p.Leu201Ile(p.L201I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000342315
Start	113005180:113005180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780389811
CDS Mutation	c.1426G>A
AA Mutation	p.Glu476Lys(p.E476K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000342315
Start	112987241:112987241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.381C>A
AA Mutation	p.Phe127Leu(p.F127L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000342315
Start	113010427:113010427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2103G>T
AA Mutation	p.Glu701Asp(p.E701D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000342315
Start	112978763:112978763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.155C>A
AA Mutation	p.Pro52His(p.P52H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000342315
Start	112997711:112997711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.819T>G
AA Mutation	p.Asp273Glu(p.D273E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000342315
Start	113007825:113007825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1777C>T
AA Mutation	p.Arg593Trp(p.R593W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000342315
Start	113004938:113004938(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1184G>T
AA Mutation	p.Gly395Val(p.G395V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000342315
Start	112995329:112995329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.482G>A
AA Mutation	p.Arg161Gln(p.R161Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000342315
Start	112997551:112997551(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.659T>G
AA Mutation	p.Leu220Arg(p.L220R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000342315
Start	113005064:113005064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1310A>G
AA Mutation	p.Glu437Gly(p.E437G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000342315
Start	113003071:113003071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748498814
CDS Mutation	c.1148G>A
AA Mutation	p.Arg383Gln(p.R383Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000342315
Start	113006564:113006564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1620G>T
AA Mutation	p.Lys540Asn(p.K540N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000342315
Start	113004982:113004982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1228G>A
AA Mutation	p.Asp410Asn(p.D410N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000342315
Start	112997557:112997557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141277168
CDS Mutation	c.665C>T
AA Mutation	p.Pro222Leu(p.P222L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000342315
Start	112997526:112997526(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.640delA
AA Mutation	p.Ile214SerfsTer41(p.I214Sfs*41)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000342315
Start	113005025:113005025(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs781171419
CDS Mutation	c.1277delA
AA Mutation	p.Asn426ThrfsTer14(p.N426Tfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000342315
Start	112987259:112987259(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.404delA
AA Mutation	p.Asn135IlefsTer15(p.N135Ifs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000342315
Start	113006482:113006483(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1540dupG
AA Mutation	p.Asp514GlyfsTer41(p.D514Gfs*41)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> OAS2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000342315
Start	113007826:113007826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs541036111
CDS Mutation	c.1778G>A
AA Mutation	p.Arg593Gln(p.R593Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000342315
Start	113004946:113004946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143746502
CDS Mutation	c.1192G>A
AA Mutation	p.Ala398Thr(p.A398T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000342315
Start	113009154:113009154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1963C>A
AA Mutation	p.Leu655Ile(p.L655I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000342315
Start	112995412:112995412(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.565T>A
AA Mutation	p.Phe189Ile(p.F189I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript