Colon Cancer: Gene >> PTPRB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261266
Start	70552840:70552840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758187856
CDS Mutation	c.4670G>A
AA Mutation	p.Gly1557Glu(p.G1557E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261266
Start	70555914:70555914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4295T>A
AA Mutation	p.Met1432Lys(p.M1432K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261266
Start	70571827:70571827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2449A>G
AA Mutation	p.Thr817Ala(p.T817A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261266
Start	70609266:70609266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.128T>C
AA Mutation	p.Ile43Thr(p.I43T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261266
Start	70576453:70576453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2117G>A
AA Mutation	p.Arg706His(p.R706H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000261266
Start	70596103:70596103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.550A>G
AA Mutation	p.Thr184Ala(p.T184A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000261266
Start	70587061:70587061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1603G>A
AA Mutation	p.Val535Ile(p.V535I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000261266
Start	70571203:70571203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761781340
CDS Mutation	c.2539G>A
AA Mutation	p.Asp847Asn(p.D847N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000261266
Start	70594526:70594526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.803T>A
AA Mutation	p.Leu268His(p.L268H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000334414
Start	70635914:70635914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.208G>A
AA Mutation	p.Ala70Thr(p.A70T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000261266
Start	70552877:70552877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4633A>G
AA Mutation	p.Asn1545Asp(p.N1545D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000334414
Start	70622487:70622487(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.611G>A
AA Mutation	p.Ser204Asn(p.S204N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000261266
Start	70566533:70566533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201608033
CDS Mutation	c.3152A>C
AA Mutation	p.Lys1051Thr(p.K1051T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000261266
Start	70589995:70589995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1365G>T
AA Mutation	p.Leu455Phe(p.L455F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000261266
Start	70560806:70560806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3643A>C
AA Mutation	p.Lys1215Gln(p.K1215Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000261266
Start	70555269:70555269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4380G>T
AA Mutation	p.Lys1460Asn(p.K1460N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000261266
Start	70524534:70524534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755804282
CDS Mutation	c.5908C>T
AA Mutation	p.Arg1970Trp(p.R1970W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000334414
Start	70635742:70635742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.380T>C
AA Mutation	p.Leu127Pro(p.L127P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261266
Start	70596284:70596284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368470501
CDS Mutation	c.369G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261266
Start	70569769:70569769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372359958
CDS Mutation	c.2886G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261266
Start	70592508:70592508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.900T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261266
Start	70563067:70563067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3291C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261266
Start	70571096:70571096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2646C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334414
Start	70622603:70622603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374992257
CDS Mutation	c.495G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000334414
Start	70622593:70622593(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.505delC
AA Mutation	p.Gln169ArgfsTer46(p.Q169Rfs*46)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261266
Start	70590158:70590158(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1202delC
AA Mutation	p.Pro401LeufsTer55(p.P401Lfs*55)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261266
Start	70555303:70555303(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.4346delC
AA Mutation	p.Pro1449LeufsTer9(p.P1449Lfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	stop_gained
Transcription ID	ENST00000261266
Start	70587226:70587226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1438G>T
AA Mutation	p.Glu480Ter(p.E480*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261266
Start	70571966:70571967(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2309dupA
AA Mutation	p.Asn770LysfsTer7(p.N770Kfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> PTPRB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000334414
Start	70622625:70622625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs549500865
CDS Mutation	c.473C>T
AA Mutation	p.Ser158Leu(p.S158L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261266
Start	70539695:70539695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5054T>C
AA Mutation	p.Ile1685Thr(p.I1685T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000334414
Start	70635827:70635827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759344115
CDS Mutation	c.295G>A
AA Mutation	p.Glu99Lys(p.E99K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261266
Start	70538948:70538948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5191A>C
AA Mutation	p.Asn1731His(p.N1731H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261266
Start	70581134:70581134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1826G>A
AA Mutation	p.Ser609Asn(p.S609N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261266
Start	70536067:70536067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5385T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261266
Start	70592325:70592325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1083C>A
Mutation Classification	Silent
Feature Type	Transcript