Colon Cancer: Gene >> PTPRG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000474889
Start	62157118:62157118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs577302571
CDS Mutation	c.734C>T
AA Mutation	p.Ser245Phe(p.S245F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000474889
Start	62203373:62203373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1578C>G
AA Mutation	p.Ile526Met(p.I526M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000474889
Start	62231261:62231261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2325A>C
AA Mutation	p.Arg775Ser(p.R775S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000474889
Start	62267748:62267748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2803T>G
AA Mutation	p.Phe935Val(p.F935V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000474889
Start	62277041:62277041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375459395
CDS Mutation	c.3629A>G
AA Mutation	p.Tyr1210Cys(p.Y1210C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000474889
Start	62272960:62272960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3197G>C
AA Mutation	p.Arg1066Thr(p.R1066T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000474889
Start	62269135:62269135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773599761
CDS Mutation	c.2975G>A
AA Mutation	p.Arg992His(p.R992H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000474889
Start	62203200:62203200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371587393
CDS Mutation	c.1405G>A
AA Mutation	p.Asp469Asn(p.D469N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000474889
Start	61989661:61989661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.227T>C
AA Mutation	p.Val76Ala(p.V76A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000474889
Start	62267756:62267756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2811G>T
AA Mutation	p.Arg937Ser(p.R937S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000474889
Start	61989707:61989707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.273G>C
AA Mutation	p.Gln91His(p.Q91H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000474889
Start	61748961:61748961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753443145
CDS Mutation	c.169G>A
AA Mutation	p.Asp57Asn(p.D57N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000474889
Start	61562328:61562328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.41T>C
AA Mutation	p.Leu14Pro(p.L14P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000474889
Start	62292536:62292536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765112298
CDS Mutation	c.4171C>T
AA Mutation	p.Pro1391Ser(p.P1391S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000474889
Start	61989691:61989691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776898840
CDS Mutation	c.257T>C
AA Mutation	p.Ile86Thr(p.I86T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000474889
Start	62218942:62218942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376160752
CDS Mutation	c.2247C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000474889
Start	62277039:62277039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3627T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000474889
Start	62277045:62277045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3633C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000474889
Start	62203925:62203925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2130C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000474889
Start	62269133:62269133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2973T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000474889
Start	62218879:62218879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2184C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000474889
Start	62282754:62282754(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3942delT
AA Mutation	p.Gln1315SerfsTer12(p.Q1315Sfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	stop_gained
Transcription ID	ENST00000474889
Start	62271461:62271461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3088G>T
AA Mutation	p.Gly1030Ter(p.G1030*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	stop_gained
Transcription ID	ENST00000474889
Start	62273824:62273824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3445C>T
AA Mutation	p.Arg1149Ter(p.R1149*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000474889
Start	62281605:62281606(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.3809_3816dupTGAACTGT
AA Mutation	p.Glu1273Ter(p.E1273*)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000474889
Start	62243806:62243807(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2379dupA
AA Mutation	p.Cys794MetfsTer20(p.C794Mfs*20)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000474889
Start	62262891:62262892(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2653_2654insAAACAAAGGAA
AA Mutation	p.Ala885GlufsTer11(p.A885Efs*11)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> PTPRG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000474889
Start	62269134:62269134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772358512
CDS Mutation	c.2974C>T
AA Mutation	p.Arg992Cys(p.R992C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000474889
Start	62277035:62277035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3623C>A
AA Mutation	p.Ala1208Asp(p.A1208D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000474889
Start	62078234:62078234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374241237
CDS Mutation	c.591C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000474889
Start	62078249:62078250(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.612dupT
AA Mutation	p.Gln205SerfsTer24(p.Q205Sfs*24)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript