Colon Cancer: Gene >> PTPN4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263708
Start	119809864:119809864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748499258
CDS Mutation	c.11G>A
AA Mutation	p.Arg4His(p.R4H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263708
Start	119882119:119882119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.436G>A
AA Mutation	p.Ala146Thr(p.A146T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263708
Start	119877502:119877502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.328T>G
AA Mutation	p.Phe110Val(p.F110V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263708
Start	119951978:119951978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1662C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263708
Start	119882558:119882558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.522T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263708
Start	119885843:119885843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.636T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263708
Start	119920197:119920197(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.963delT
AA Mutation	p.Phe321LeufsTer7(p.F321Lfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263708
Start	119881795:119881795(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.383delT
AA Mutation	p.Leu128CysfsTer22(p.L128Cfs*22)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000263708
Start	119934837:119934837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1234C>T
AA Mutation	p.Arg412Ter(p.R412*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000263708
Start	119952120:119952120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1804C>T
AA Mutation	p.Arg602Ter(p.R602*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained;frameshift_variant
Transcription ID	ENST00000263708
Start	119882609:119882610(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.573_574insTTATAGT
AA Mutation	p.His192LeufsTer2(p.H192Lfs*2)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263708
Start	119882610:119882611(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.575_576insAA
AA Mutation	p.His192GlnfsTer6(p.H192Qfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263708
Start	119915209:119915210(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.795_796insT
AA Mutation	p.Lys266Ter(p.K266*)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000263708
Start	119934959:119934959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147418905
CDS Mutation	c.1355+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> PTPN4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263708
Start	119956929:119956929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143662385
CDS Mutation	c.2066C>T
AA Mutation	p.Ser689Leu(p.S689L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263708
Start	119882514:119882514(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.478G>T
AA Mutation	p.Asp160Tyr(p.D160Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263708
Start	119965567:119965567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779244973
CDS Mutation	c.2480C>T
AA Mutation	p.Ser827Leu(p.S827L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000263708
Start	119809900:119809900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.47G>A
AA Mutation	p.Arg16Gln(p.R16Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000263708
Start	119915221:119915221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.807T>G
AA Mutation	p.Phe269Leu(p.F269L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263708
Start	119932511:119932511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1158A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000263708
Start	119885850:119885850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.643G>T
AA Mutation	p.Glu215Ter(p.E215*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000263708
Start	119882108:119882110(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.427_429delTCT
AA Mutation	p.Ser143del(p.S143del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript