Colon Cancer: Gene >> PRX

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000324001
Start	40394052:40394052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767488196
CDS Mutation	c.4300C>T
AA Mutation	p.Arg1434Trp(p.R1434W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000324001
Start	40397960:40397960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781394276
CDS Mutation	c.392G>A
AA Mutation	p.Ser131Asn(p.S131N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000324001
Start	40396958:40396958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1394T>A
AA Mutation	p.Leu465His(p.L465H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000324001
Start	40394145:40394145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139051512
CDS Mutation	c.4207G>A
AA Mutation	p.Val1403Ile(p.V1403I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000324001
Start	40395018:40395018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3334G>A
AA Mutation	p.Ala1112Thr(p.A1112T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000324001
Start	40395036:40395036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776889377
CDS Mutation	c.3316G>A
AA Mutation	p.Ala1106Thr(p.A1106T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000324001
Start	40396883:40396883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752314625
CDS Mutation	c.1469G>A
AA Mutation	p.Arg490Gln(p.R490Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000324001
Start	40395533:40395533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2819G>A
AA Mutation	p.Gly940Glu(p.G940E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000324001
Start	40394433:40394433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752593001
CDS Mutation	c.3919C>T
AA Mutation	p.Arg1307Trp(p.R1307W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000324001
Start	40397852:40397852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757322355
CDS Mutation	c.500G>A
AA Mutation	p.Arg167His(p.R167H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000324001
Start	40396368:40396368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1984G>A
AA Mutation	p.Val662Ile(p.V662I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324001
Start	40397059:40397059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1293G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324001
Start	40394035:40394035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372280596
CDS Mutation	c.4317C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324001
Start	40394146:40394146(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771992595
CDS Mutation	c.4206C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000324001
Start	40394579:40394579(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3773delG
AA Mutation	p.Gly1258AlafsTer124(p.G1258Afs*124)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000324001
Start	40397349:40397349(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1003delG
AA Mutation	p.Val335TrpfsTer21(p.V335Wfs*21)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000324001
Start	40397787:40397787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.565C>T
AA Mutation	p.Gln189Ter(p.Q189*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PRX

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324001
Start	40394167:40394167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4185C>T
Mutation Classification	Silent
Feature Type	Transcript