Colon Cancer: Gene >> AOC3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000308423
Start	42852689:42852689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1346C>T
AA Mutation	p.Ser449Leu(p.S449L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000308423
Start	42851799:42851799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.456G>T
AA Mutation	p.Met152Ile(p.M152I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000308423
Start	42856489:42856489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2231A>C
AA Mutation	p.Gln744Pro(p.Q744P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000308423
Start	42851723:42851723(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.380T>C
AA Mutation	p.Ile127Thr(p.I127T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000308423
Start	42852451:42852451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1108G>A
AA Mutation	p.Ala370Thr(p.A370T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000308423
Start	42851725:42851725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762768941
CDS Mutation	c.382G>A
AA Mutation	p.Val128Ile(p.V128I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000308423
Start	42852668:42852668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757517219
CDS Mutation	c.1325G>A
AA Mutation	p.Arg442Gln(p.R442Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308423
Start	42856460:42856460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756306820
CDS Mutation	c.2202C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308423
Start	42852912:42852912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1569C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308423
Start	42856304:42856304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2046T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308423
Start	42852831:42852831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1488C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308423
Start	42856418:42856418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753309316
CDS Mutation	c.2160C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000308423
Start	42855521:42855521(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1968delC
AA Mutation	p.Thr657LeufsTer22(p.T657Lfs*22)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000308423
Start	42856374:42856374(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758238458
CDS Mutation	c.2116C>T
AA Mutation	p.Arg706Ter(p.R706*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000308423
Start	42854594:42854595(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1751dupC
AA Mutation	p.Arg585SerfsTer60(p.R585Sfs*60)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> AOC3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000308423
Start	42852224:42852224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.881A>T
AA Mutation	p.Asn294Ile(p.N294I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000308423
Start	42854658:42854658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs555331668
CDS Mutation	c.1811G>A
AA Mutation	p.Arg604His(p.R604H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308423
Start	42852477:42852477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1134A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308423
Start	42852690:42852690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs115107156
CDS Mutation	c.1347G>A
Mutation Classification	Silent
Feature Type	Transcript