Colon Cancer: Gene >> PTPN3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374541
Start	109389340:109389340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763936455
CDS Mutation	c.2146G>A
AA Mutation	p.Ala716Thr(p.A716T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374541
Start	109410009:109410009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1568T>G
AA Mutation	p.Phe523Cys(p.F523C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374541
Start	109463419:109463419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147740778
CDS Mutation	c.16C>T
AA Mutation	p.Arg6Cys(p.R6C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000374541
Start	109438184:109438184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772217385
CDS Mutation	c.517G>A
AA Mutation	p.Asp173Asn(p.D173N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000374541
Start	109422786:109422786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1068A>T
AA Mutation	p.Arg356Ser(p.R356S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000374541
Start	109383517:109383517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2288A>G
AA Mutation	p.Asp763Gly(p.D763G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000374541
Start	109379614:109379614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2684G>T
AA Mutation	p.Cys895Phe(p.C895F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000374541
Start	109406617:109406617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1637C>T
AA Mutation	p.Ala546Val(p.A546V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000374541
Start	109436959:109436959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.599A>G
AA Mutation	p.Gln200Arg(p.Q200R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000374541
Start	109463424:109463424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765688707
CDS Mutation	c.11G>A
AA Mutation	p.Arg4Gln(p.R4Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000374541
Start	109381667:109381667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2649G>A
AA Mutation	p.Met883Ile(p.M883I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000374541
Start	109427052:109427052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.899C>T
AA Mutation	p.Ser300Phe(p.S300F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374541
Start	109436925:109436925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143196464
CDS Mutation	c.633G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374541
Start	109404472:109404472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1929C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000374541
Start	109422764:109422764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1090G>T
AA Mutation	p.Glu364Ter(p.E364*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000374541
Start	109420533:109420533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1204G>T
AA Mutation	p.Glu402Ter(p.E402*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000374541
Start	109420599:109420599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1138C>T
AA Mutation	p.Arg380Ter(p.R380*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374541
Start	109391544:109391545(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1970dupA
AA Mutation	p.Pro658AlafsTer20(p.P658Afs*20)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000374541
Start	109382449:109382449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2383-2A>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> PTPN3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374541
Start	109391161:109391161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2083T>G
AA Mutation	p.Tyr695Asp(p.Y695D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374541
Start	109433133:109433133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.704G>A
AA Mutation	p.Gly235Glu(p.G235E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript