Colon Cancer: Gene >> PTPRN2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000389418
Start	157656431:157656431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2122C>T
AA Mutation	p.Arg708Cys(p.R708C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000389418
Start	158167285:158167285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.556G>T
AA Mutation	p.Asp186Tyr(p.D186Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000389418
Start	158167032:158167032(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751826612
CDS Mutation	c.809G>A
AA Mutation	p.Arg270His(p.R270H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000389418
Start	157568925:157568925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2879T>C
AA Mutation	p.Met960Thr(p.M960T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000389418
Start	157568929:157568929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2875G>A
AA Mutation	p.Asp959Asn(p.D959N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000389418
Start	158081343:158081343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201100433
CDS Mutation	c.1678G>A
AA Mutation	p.Ala560Thr(p.A560T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000389418
Start	157656430:157656430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369227370
CDS Mutation	c.2123G>A
AA Mutation	p.Arg708His(p.R708H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000389418
Start	157682856:157682856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775228380
CDS Mutation	c.1870G>A
AA Mutation	p.Ala624Thr(p.A624T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000389418
Start	158136666:158136666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1162C>T
AA Mutation	p.Leu388Phe(p.L388F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000389418
Start	158134035:158134035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146255697
CDS Mutation	c.1198G>A
AA Mutation	p.Gly400Arg(p.G400R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000389418
Start	158192380:158192380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.496G>A
AA Mutation	p.Ala166Thr(p.A166T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000389418
Start	157682825:157682825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771062413
CDS Mutation	c.1901G>A
AA Mutation	p.Gly634Asp(p.G634D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000389418
Start	157548995:157548995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2927C>T
AA Mutation	p.Ala976Val(p.A976V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000389418
Start	157578083:157578083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373071385
CDS Mutation	c.2554G>A
AA Mutation	p.Gly852Ser(p.G852S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000389418
Start	158136690:158136690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144837405
CDS Mutation	c.1138G>A
AA Mutation	p.Gly380Arg(p.G380R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000389418
Start	157656442:157656442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2111G>T
AA Mutation	p.Ser704Ile(p.S704I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389418
Start	158192429:158192429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769707155
CDS Mutation	c.447C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389418
Start	158133832:158133832(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772404937
CDS Mutation	c.1401C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389418
Start	158081365:158081365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1656A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389418
Start	158138400:158138400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769163767
CDS Mutation	c.1026C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389418
Start	157549000:157549000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370473762
CDS Mutation	c.2922C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389418
Start	157595301:157595301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139627101
CDS Mutation	c.2433G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000389418
Start	158136657:158136657(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1171G>T
AA Mutation	p.Glu391Ter(p.E391*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	stop_gained
Transcription ID	ENST00000389418
Start	158133906:158133906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1327G>T
AA Mutation	p.Gly443Ter(p.G443*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000389418
Start	158166984:158166985(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.856dupC
AA Mutation	p.Gln286ProfsTer35(p.Q286Pfs*35)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> PTPRN2

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389418
Start	157549000:157549000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370473762
CDS Mutation	c.2922C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389418
Start	158133691:158133691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201964824
CDS Mutation	c.1542C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389418
Start	158110876:158110876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374889194
CDS Mutation	c.1596C>T
Mutation Classification	Silent
Feature Type	Transcript