Colon Cancer: Gene >> AGO3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373191
Start	36039922:36039922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1975C>T
AA Mutation	p.Arg659Trp(p.R659W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373191
Start	36055693:36055693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2531C>T
AA Mutation	p.Ala844Val(p.A844V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373191
Start	35972154:35972154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.443C>T
AA Mutation	p.Pro148Leu(p.P148L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000373191
Start	36043507:36043507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2233T>C
AA Mutation	p.Tyr745His(p.Y745H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000373191
Start	35972228:35972228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.517A>G
AA Mutation	p.Met173Val(p.M173V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000373191
Start	36034228:36034228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1646A>G
AA Mutation	p.Gln549Arg(p.Q549R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000373191
Start	36009579:36009579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1134G>T
AA Mutation	p.Glu378Asp(p.E378D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000373191
Start	36054949:36054949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2278A>G
AA Mutation	p.Thr760Ala(p.T760A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000373191
Start	36008729:36008729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.833G>A
AA Mutation	p.Arg278Gln(p.R278Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000373191
Start	36013714:36013714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1234C>T
AA Mutation	p.Arg412Cys(p.R412C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000373191
Start	36036249:36036249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1824G>T
AA Mutation	p.Lys608Asn(p.K608N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000373191
Start	36004446:36004446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.764A>G
AA Mutation	p.His255Arg(p.H255R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000373191
Start	35967008:35967008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754906872
CDS Mutation	c.245G>A
AA Mutation	p.Arg82His(p.R82H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373191
Start	36043503:36043503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2229C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000373191
Start	35972066:35972066(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.355C>T
AA Mutation	p.Arg119Ter(p.R119*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000373191
Start	36040311:36040311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2042T>G
AA Mutation	p.Leu681Ter(p.L681*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373191
Start	35973395:35973396(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.543dupA
AA Mutation	p.Phe182IlefsTer9(p.F182Ifs*9)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> AGO3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373191
Start	35973508:35973508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.655G>A
AA Mutation	p.Asp219Asn(p.D219N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373191
Start	36013716:36013716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759485254
CDS Mutation	c.1236C>T
Mutation Classification	Silent
Feature Type	Transcript