Colon Cancer: Gene >> PER3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361923
Start	7826630:7826630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2084G>A
AA Mutation	p.Arg695Gln(p.R695Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361923
Start	7827348:7827348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2395G>A
AA Mutation	p.Val799Ile(p.V799I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361923
Start	7827756:7827756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2803C>T
AA Mutation	p.Pro935Ser(p.P935S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361923
Start	7809903:7809903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1250T>C
AA Mutation	p.Val417Ala(p.V417A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000361923
Start	7801118:7801118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs559444285
CDS Mutation	c.796C>T
AA Mutation	p.Arg266Trp(p.R266W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000361923
Start	7835906:7835906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs35802556
CDS Mutation	c.3332C>T
AA Mutation	p.Thr1111Ile(p.T1111I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000361923
Start	7784993:7784993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.116A>G
AA Mutation	p.Asp39Gly(p.D39G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000361923
Start	7785536:7785536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.224G>A
AA Mutation	p.Ser75Asn(p.S75N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000361923
Start	7794007:7794007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs114300822
CDS Mutation	c.640C>T
AA Mutation	p.Arg214Cys(p.R214C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000361923
Start	7827348:7827348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2395G>T
AA Mutation	p.Val799Phe(p.V799F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000361923
Start	7810543:7810543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1474A>C
AA Mutation	p.Thr492Pro(p.T492P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000361923
Start	7788123:7788123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375445968
CDS Mutation	c.469C>T
AA Mutation	p.Arg157Cys(p.R157C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000361923
Start	7809963:7809963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1310G>A
AA Mutation	p.Ser437Asn(p.S437N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000361923
Start	7842703:7842703(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3554C>T
AA Mutation	p.Ala1185Val(p.A1185V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000361923
Start	7827798:7827798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2845T>C
AA Mutation	p.Cys949Arg(p.C949R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000361923
Start	7827372:7827372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775310427
CDS Mutation	c.2419G>A
AA Mutation	p.Ala807Thr(p.A807T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000361923
Start	7810543:7810543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1474A>G
AA Mutation	p.Thr492Ala(p.T492A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000361923
Start	7788104:7788104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.450G>T
AA Mutation	p.Gln150His(p.Q150H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000361923
Start	7788138:7788138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.484C>A
AA Mutation	p.Leu162Met(p.L162M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361923
Start	7788194:7788194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs535936436
CDS Mutation	c.540C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000361923
Start	7785454:7785454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.142C>T
AA Mutation	p.Arg48Ter(p.R48*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361923
Start	7827691:7827692(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2738_2739insTGATATC
AA Mutation	p.His914AspfsTer28(p.H914Dfs*28)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> PER3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361923
Start	7829841:7829841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2867T>G
AA Mutation	p.Val956Gly(p.V956G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000361923
Start	7826548:7826548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2002G>T
AA Mutation	p.Glu668Ter(p.E668*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript