Colon Cancer: Gene >> AGO2

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000220592
Start	140555897:140555897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1268G>A
AA Mutation	p.Arg423Lys(p.R423K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000220592
Start	140549209:140549209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1493C>T
AA Mutation	p.Ala498Val(p.A498V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000220592
Start	140539426:140539426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2063G>A
AA Mutation	p.Arg688His(p.R688H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000220592
Start	140585119:140585119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.215G>T
AA Mutation	p.Arg72Met(p.R72M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000220592
Start	140541228:140541228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1970C>T
AA Mutation	p.Thr657Met(p.T657M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000220592
Start	140549237:140549237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1465C>T
AA Mutation	p.Pro489Ser(p.P489S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000220592
Start	140558539:140558539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.824T>C
AA Mutation	p.Met275Thr(p.M275T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000220592
Start	140549218:140549218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1484C>T
AA Mutation	p.Ala495Val(p.A495V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000220592
Start	140544289:140544289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1763A>G
AA Mutation	p.Gln588Arg(p.Q588R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000220592
Start	140551417:140551417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1289C>T
AA Mutation	p.Pro430Leu(p.P430L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000220592
Start	140557206:140557206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.909G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000220592
Start	140535501:140535501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2238C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000220592
Start	140585289:140585289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.45G>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000220592
Start	140559516:140559516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767782553
CDS Mutation	c.669G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000220592
Start	140562482:140562482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs76003517
CDS Mutation	c.489C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000220592
Start	140555900:140555900(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1265delG
AA Mutation	p.Gly422AlafsTer46(p.G422Afs*46)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000220592
Start	140556248:140556248(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1065delA
AA Mutation	p.Lys355AsnfsTer2(p.K355Nfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000220592
Start	140539428:140539429(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2060dupT
AA Mutation	p.Arg688ProfsTer2(p.R688Pfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> AGO2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000220592
Start	140555934:140555934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1231C>T
AA Mutation	p.Arg411Trp(p.R411W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000220592
Start	140539385:140539385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2104A>C
AA Mutation	p.Ile702Leu(p.I702L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000220592
Start	140547625:140547625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1591G>A
AA Mutation	p.Glu531Lys(p.E531K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript