Colon Cancer: Gene >> AOC2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000253799
Start	42845458:42845458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.832G>T
AA Mutation	p.Gly278Cys(p.G278C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000253799
Start	42844847:42844847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376064787
CDS Mutation	c.221G>A
AA Mutation	p.Arg74Gln(p.R74Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000253799
Start	42849227:42849227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1730G>T
AA Mutation	p.Ser577Ile(p.S577I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000253799
Start	42845756:42845756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1130G>A
AA Mutation	p.Arg377His(p.R377H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000253799
Start	42845961:42845961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1335C>A
AA Mutation	p.Phe445Leu(p.F445L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000253799
Start	42845738:42845738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1112C>T
AA Mutation	p.Pro371Leu(p.P371L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000253799
Start	42845120:42845120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145007333
CDS Mutation	c.494G>A
AA Mutation	p.Arg165His(p.R165H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000253799
Start	42849182:42849182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1685G>A
AA Mutation	p.Arg562Gln(p.R562Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000253799
Start	42845329:42845329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.703C>T
AA Mutation	p.His235Tyr(p.H235Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000253799
Start	42845772:42845772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1146C>A
AA Mutation	p.Ser382Arg(p.S382R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000253799
Start	42845447:42845447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.821A>C
AA Mutation	p.Glu274Ala(p.E274A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000253799
Start	42845930:42845930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764975824
CDS Mutation	c.1304G>A
AA Mutation	p.Arg435Gln(p.R435Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000253799
Start	42849287:42849287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780166614
CDS Mutation	c.1790G>A
AA Mutation	p.Arg597His(p.R597H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000253799
Start	42845828:42845828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1202A>G
AA Mutation	p.Gln401Arg(p.Q401R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000253799
Start	42845813:42845813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1187T>A
AA Mutation	p.Val396Glu(p.V396E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253799
Start	42846087:42846087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1461T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253799
Start	42845433:42845433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.807C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000253799
Start	42845549:42845567(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.926_944delAGTTCTCGCCCCAGGGTTC
AA Mutation	p.Gln309ProfsTer27(p.Q309Pfs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000253799
Start	42844965:42844965(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.344delC
AA Mutation	p.Pro115HisfsTer20(p.P115Hfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000253799
Start	42849091:42849091(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1598delA
AA Mutation	p.Asn533ThrfsTer4(p.N533Tfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000253799
Start	42845929:42845929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777111912
CDS Mutation	c.1303C>T
AA Mutation	p.Arg435Ter(p.R435*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> AOC2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000253799
Start	42845471:42845471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.845T>C
AA Mutation	p.Val282Ala(p.V282A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript