Colon Cancer: Gene >> AOC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360937
Start	150857798:150857798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1328C>T
AA Mutation	p.Ala443Val(p.A443V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000360937
Start	150857497:150857497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774495004
CDS Mutation	c.1027G>A
AA Mutation	p.Gly343Arg(p.G343R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000360937
Start	150857467:150857467(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757908154
CDS Mutation	c.997G>A
AA Mutation	p.Gly333Arg(p.G333R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000360937
Start	150857060:150857060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761385425
CDS Mutation	c.590G>A
AA Mutation	p.Arg197His(p.R197H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000360937
Start	150857611:150857611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752373263
CDS Mutation	c.1141G>A
AA Mutation	p.Val381Ile(p.V381I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000360937
Start	150856990:150856990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.520T>C
AA Mutation	p.Phe174Leu(p.F174L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360937
Start	150857307:150857307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.837G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360937
Start	150861131:150861131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2178C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000360937
Start	150857033:150857033(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.568delC
AA Mutation	p.Arg190GlyfsTer18(p.R190Gfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000360937
Start	150861171:150861171(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2222delC
AA Mutation	p.Pro741LeufsTer54(p.P741Lfs*54)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> AOC1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360937
Start	150857493:150857493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs553084982
CDS Mutation	c.1023C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360937
Start	150856636:150856636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.166C>T
Mutation Classification	Silent
Feature Type	Transcript