Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> PTPN14

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000366956
Start	214384261:214384261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373438300
CDS Mutation	c.1594G>A
AA Mutation	p.Ala532Thr(p.A532T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000366956
Start	214384461:214384461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1394C>T
AA Mutation	p.Ser465Phe(p.S465F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000366956
Start	214377998:214377998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771521435
CDS Mutation	c.2649G>T
AA Mutation	p.Glu883Asp(p.E883D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000366956
Start	214451912:214451912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.237G>T
AA Mutation	p.Glu79Asp(p.E79D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000366956
Start	214383384:214383384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2471C>A
AA Mutation	p.Pro824His(p.P824H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000366956
Start	214372781:214372781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2966C>T
AA Mutation	p.Thr989Met(p.T989M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000366956
Start	214383550:214383550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2305G>A
AA Mutation	p.Ala769Thr(p.A769T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000366956
Start	214384057:214384057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775147296
CDS Mutation	c.1798C>T
AA Mutation	p.Arg600Trp(p.R600W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000366956
Start	214384593:214384593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771815955
CDS Mutation	c.1262T>C
AA Mutation	p.Met421Thr(p.M421T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000366956
Start	214372730:214372730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3017C>T
AA Mutation	p.Ala1006Val(p.A1006V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000366956
Start	214384141:214384141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200947677
CDS Mutation	c.1714C>T
AA Mutation	p.Arg572Trp(p.R572W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000366956
Start	214384282:214384282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1573C>A
AA Mutation	p.Pro525Thr(p.P525T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000366956
Start	214369517:214369517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3211C>T
AA Mutation	p.His1071Tyr(p.H1071Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000366956
Start	214357954:214357954(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3532A>G
AA Mutation	p.Ile1178Val(p.I1178V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000366956
Start	214383756:214383756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2099A>G
AA Mutation	p.Asp700Gly(p.D700G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000366956
Start	214376250:214376250(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2876A>G
AA Mutation	p.Asn959Ser(p.N959S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000366956
Start	214464750:214464750(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.54G>T
AA Mutation	p.Lys18Asn(p.K18N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000366956
Start	214369594:214369594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs181559516
CDS Mutation	c.3134G>A
AA Mutation	p.Arg1045Gln(p.R1045Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000366956
Start	214376415:214376415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2711T>C
AA Mutation	p.Leu904Pro(p.L904P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366956
Start	214376291:214376291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2835T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366956
Start	214384352:214384352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1503G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366956
Start	214384655:214384655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs12404313
CDS Mutation	c.1200G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366956
Start	214384559:214384559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1296C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366956
Start	214378054:214378054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2593C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366956
Start	214384070:214384070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766987506
CDS Mutation	c.1785G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366956
Start	214464696:214464696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748318666
CDS Mutation	c.108G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366956
Start	214384148:214384148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1707C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366956
Start	214383514:214383514(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2341C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000366956
Start	214384148:214384148(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1707delC
AA Mutation	p.Tyr570ThrfsTer29(p.Y570Tfs*29)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	stop_gained
Transcription ID	ENST00000366956
Start	214369667:214369667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771183448
CDS Mutation	c.3061C>T
AA Mutation	p.Arg1021Ter(p.R1021*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	stop_gained
Transcription ID	ENST00000366956
Start	214393732:214393732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.892C>T
AA Mutation	p.Arg298Ter(p.R298*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000366956
Start	214391023:214391024(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.951dupC
AA Mutation	p.Ile318HisfsTer29(p.I318Hfs*29)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000366956
Start	214383321:214383322(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2532_2533dupGA
AA Mutation	p.Met845ArgfsTer2(p.M845Rfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000366956
Start	214414727:214414727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.345-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> PTPN14

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000366956
Start	214378003:214378003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2644G>A
AA Mutation	p.Glu882Lys(p.E882K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000366956
Start	214391017:214391017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750538905
CDS Mutation	c.958C>T
AA Mutation	p.Arg320Cys(p.R320C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000366956
Start	214384506:214384506(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1349G>A
AA Mutation	p.Arg450His(p.R450H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000366956
Start	214451900:214451900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.249G>T
AA Mutation	p.Lys83Asn(p.K83N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000366956
Start	214357984:214357984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766848166
CDS Mutation	c.3502G>A
AA Mutation	p.Ala1168Thr(p.A1168T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000366956
Start	214364640:214364640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3307A>G
AA Mutation	p.Thr1103Ala(p.T1103A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366956
Start	214391020:214391020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.955A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366956
Start	214376363:214376363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146527644
CDS Mutation	c.2763G>A
Mutation Classification	Silent
Feature Type	Transcript