Colon Cancer: Gene >> PTPRH

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376350
Start	55202170:55202170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750050374
CDS Mutation	c.1039G>A
AA Mutation	p.Ala347Thr(p.A347T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000376350
Start	55198691:55198691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368354556
CDS Mutation	c.1642G>A
AA Mutation	p.Glu548Lys(p.E548K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000376350
Start	55200446:55200446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1210C>A
AA Mutation	p.Leu404Ile(p.L404I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000376350
Start	55197318:55197318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371152156
CDS Mutation	c.1789G>A
AA Mutation	p.Val597Ile(p.V597I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000376350
Start	55204036:55204036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.632T>C
AA Mutation	p.Val211Ala(p.V211A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000376350
Start	55181785:55181785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3317C>T
AA Mutation	p.Ala1106Val(p.A1106V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000376350
Start	55205369:55205369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.576G>T
AA Mutation	p.Lys192Asn(p.K192N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000376350
Start	55187543:55187543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs575359835
CDS Mutation	c.2536G>A
AA Mutation	p.Ala846Thr(p.A846T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000376350
Start	55181786:55181786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150929721
CDS Mutation	c.3316G>A
AA Mutation	p.Ala1106Thr(p.A1106T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000376350
Start	55203880:55203880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.788C>T
AA Mutation	p.Thr263Ile(p.T263I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000376350
Start	55181870:55181870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367809853
CDS Mutation	c.3232C>T
AA Mutation	p.Arg1078Trp(p.R1078W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000376350
Start	55205467:55205467(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.478G>T
AA Mutation	p.Gly160Cys(p.G160C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376350
Start	55198803:55198803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1530C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376350
Start	55202102:55202102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs536291307
CDS Mutation	c.1107G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376350
Start	55197190:55197190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61734205
CDS Mutation	c.1917G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376350
Start	55188087:55188087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149252651
CDS Mutation	c.2466C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376350
Start	55205516:55205516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201526534
CDS Mutation	c.429C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000376350
Start	55200276:55200277(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1379dupA
AA Mutation	p.Asn460LysfsTer60(p.N460Kfs*60)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> PTPRH

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376350
Start	55200449:55200449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760246867
CDS Mutation	c.1207G>A
AA Mutation	p.Ala403Thr(p.A403T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000376350
Start	55186529:55186529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778712446
CDS Mutation	c.2578C>T
AA Mutation	p.Arg860Trp(p.R860W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000376350
Start	55202070:55202070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769189088
CDS Mutation	c.1139G>A
AA Mutation	p.Arg380Gln(p.R380Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000376350
Start	55198853:55198853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369140474
CDS Mutation	c.1480C>T
AA Mutation	p.Arg494Cys(p.R494C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000376350
Start	55200358:55200358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753627783
CDS Mutation	c.1298G>A
AA Mutation	p.Arg433Gln(p.R433Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376350
Start	55181790:55181790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770213055
CDS Mutation	c.3312C>T
Mutation Classification	Silent
Feature Type	Transcript