Colon Cancer: Gene >> NCOA4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000581486
Start	46016610:46016610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.71G>A
AA Mutation	p.Arg24Gln(p.R24Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000581486
Start	46016611:46016611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.70C>T
AA Mutation	p.Arg24Trp(p.R24W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000581486
Start	46010593:46010593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1328C>A
AA Mutation	p.Pro443His(p.P443H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000581486
Start	46011154:46011154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.767G>A
AA Mutation	p.Gly256Asp(p.G256D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000581486
Start	46010803:46010803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1118T>C
AA Mutation	p.Leu373Ser(p.L373S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000581486
Start	46011082:46011082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.839C>T
AA Mutation	p.Ser280Phe(p.S280F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000581486
Start	46010236:46010236(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	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000581486
Start	46010677:46010677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782431324
CDS Mutation	c.1244A>T
AA Mutation	p.Glu415Val(p.E415V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000581486
Start	46016597:46016597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.84G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000581486
Start	46016588:46016588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.93T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000581486
Start	46010775:46010775(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1146delC
AA Mutation	p.Ser383AlafsTer18(p.S383Afs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000581486
Start	46010237:46010237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1684C>T
AA Mutation	p.Arg562Ter(p.R562*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> NCOA4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000581486
Start	46010236:46010236(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	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000581486
Start	46010530:46010530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1391G>T
AA Mutation	p.Arg464Ile(p.R464I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript