Colon Cancer: Gene >> DNAAF3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000524407
Start	55160745:55160745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.943A>G
AA Mutation	p.Thr315Ala(p.T315A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000524407
Start	55161645:55161645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.661G>A
AA Mutation	p.Gly221Arg(p.G221R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000524407
Start	55161325:55161325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.757C>T
AA Mutation	p.Arg253Trp(p.R253W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000524407
Start	55161726:55161726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.580C>A
AA Mutation	p.Leu194Met(p.L194M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000524407
Start	55159292:55159292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1396G>A
AA Mutation	p.Val466Ile(p.V466I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000524407
Start	55161340:55161340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.742T>C
AA Mutation	p.Tyr248His(p.Y248H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000524407
Start	55159969:55159969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1093A>C
AA Mutation	p.Asn365His(p.N365H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000524407
Start	55161696:55161696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.610G>A
AA Mutation	p.Ala204Thr(p.A204T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000524407
Start	55159926:55159926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1136G>A
AA Mutation	p.Arg379Gln(p.R379Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000524407
Start	55166342:55166342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.72C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000524407
Start	55159359:55159359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767701157
CDS Mutation	c.1329C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000524407
Start	55160713:55160713(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.975delG
AA Mutation	p.Arg326AlafsTer82(p.R326Afs*82)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000524407
Start	55160676:55160676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1012C>T
AA Mutation	p.Gln338Ter(p.Q338*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000524407
Start	55166328:55166328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.85+1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> DNAAF3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000524407
Start	55161106:55161106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.871G>A
AA Mutation	p.Asp291Asn(p.D291N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript