Colon Cancer: Gene >> PTPRF

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359947
Start	43620485:43620485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372799990
CDS Mutation	c.5270G>A
AA Mutation	p.Arg1757His(p.R1757H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359947
Start	43619392:43619392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4751G>A
AA Mutation	p.Arg1584Gln(p.R1584Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359947
Start	43591427:43591427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752774736
CDS Mutation	c.1405G>A
AA Mutation	p.Ala469Thr(p.A469T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000359947
Start	43606949:43606949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146960105
CDS Mutation	c.3838G>A
AA Mutation	p.Ala1280Thr(p.A1280T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000359947
Start	43613674:43613674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4030C>T
AA Mutation	p.Leu1344Phe(p.L1344F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000359947
Start	43598754:43598754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2154G>T
AA Mutation	p.Glu718Asp(p.E718D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000359947
Start	43618729:43618729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749935647
CDS Mutation	c.4471C>T
AA Mutation	p.Arg1491Cys(p.R1491C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000359947
Start	43603992:43603992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2840G>A
AA Mutation	p.Arg947His(p.R947H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000359947
Start	43588861:43588861(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.810G>T
AA Mutation	p.Glu270Asp(p.E270D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000359947
Start	43591503:43591503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1481T>C
AA Mutation	p.Val494Ala(p.V494A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000359947
Start	43603620:43603620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs565543436
CDS Mutation	c.2468G>A
AA Mutation	p.Arg823Gln(p.R823Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000359947
Start	43603965:43603965(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200617199
CDS Mutation	c.2813C>T
AA Mutation	p.Pro938Leu(p.P938L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000359947
Start	43569746:43569746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150660901
CDS Mutation	c.536C>T
AA Mutation	p.Thr179Met(p.T179M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000359947
Start	43605582:43605582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774648724
CDS Mutation	c.3443C>T
AA Mutation	p.Thr1148Met(p.T1148M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000359947
Start	43620839:43620839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5366A>G
AA Mutation	p.Asp1789Gly(p.D1789G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000359947
Start	43591428:43591428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1406C>T
AA Mutation	p.Ala469Val(p.A469V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359947
Start	43597884:43597884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774549273
CDS Mutation	c.1950C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359947
Start	43620894:43620894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs557292785
CDS Mutation	c.5421C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359947
Start	43603433:43603433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2358C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359947
Start	43605432:43605432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770390307
CDS Mutation	c.3378C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359947
Start	43553634:43553634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs6684279
CDS Mutation	c.234C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359947
Start	43605556:43605556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3417T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359947
Start	43617869:43617869(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200241694
CDS Mutation	c.4329G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359947
Start	43617773:43617773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746820683
CDS Mutation	c.4233C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359947
Start	43603732:43603732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772134870
CDS Mutation	c.2580C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359947
Start	43605261:43605261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3207C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PTPRF

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359947
Start	43569622:43569622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777318046
CDS Mutation	c.412G>A
AA Mutation	p.Asp138Asn(p.D138N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000359947
Start	43620578:43620578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5363G>A
AA Mutation	p.Arg1788Gln(p.R1788Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359947
Start	43619752:43619752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5005C>T
AA Mutation	p.Arg1669Trp(p.R1669W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000359947
Start	43553938:43553938(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776445536
CDS Mutation	c.376G>A
AA Mutation	p.Glu126Lys(p.E126K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359947
Start	43605333:43605333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3279C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359947
Start	43605318:43605318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3264G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359947
Start	43619176:43619176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376776266
CDS Mutation	c.4620C>T
Mutation Classification	Silent
Feature Type	Transcript