Colon Cancer: Gene >> ASAP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000336689
Start	23437225:23437225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1247G>A
AA Mutation	p.Gly416Asp(p.G416D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000336689
Start	23435856:23435856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1744G>A
AA Mutation	p.Ala582Thr(p.A582T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000336689
Start	23441672:23441672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.730G>A
AA Mutation	p.Ala244Thr(p.A244T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000336689
Start	23441205:23441205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.841C>A
AA Mutation	p.Leu281Met(p.L281M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000336689
Start	23439177:23439177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.998C>T
AA Mutation	p.Thr333Ile(p.T333I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000336689
Start	23441454:23441454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.767A>G
AA Mutation	p.Asp256Gly(p.D256G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000336689
Start	23437289:23437289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1183G>A
AA Mutation	p.Glu395Lys(p.E395K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000336689
Start	23437461:23437461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1114T>C
AA Mutation	p.Tyr372His(p.Y372H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000336689
Start	23433661:23433661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1984G>A
AA Mutation	p.Ala662Thr(p.A662T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000336689
Start	23456146:23456146(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.178C>T
AA Mutation	p.Arg60Trp(p.R60W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336689
Start	23437290:23437290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1182C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ASAP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000336689
Start	23437467:23437467(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1108C>T
AA Mutation	p.Arg370Trp(p.R370W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000336689
Start	23439226:23439226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760996705
CDS Mutation	c.949C>T
AA Mutation	p.Arg317Ter(p.R317*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000336689
Start	23442530:23442531(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.554_555dupAG
AA Mutation	p.Arg186SerfsTer21(p.R186Sfs*21)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript