Colon Cancer: Gene >> PER1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000317276
Start	8146957:8146957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1675C>A
AA Mutation	p.Gln559Lys(p.Q559K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000317276
Start	8146912:8146912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781105048
CDS Mutation	c.1720C>T
AA Mutation	p.Arg574Trp(p.R574W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000317276
Start	8141232:8141232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201015773
CDS Mutation	c.3709G>A
AA Mutation	p.Glu1237Lys(p.E1237K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000317276
Start	8143552:8143552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2786C>A
AA Mutation	p.Pro929Gln(p.P929Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000317276
Start	8149492:8149492(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.823C>A
AA Mutation	p.Leu275Met(p.L275M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000317276
Start	8149835:8149835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138547494
CDS Mutation	c.571G>A
AA Mutation	p.Glu191Lys(p.E191K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000317276
Start	8143796:8143796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2542C>A
AA Mutation	p.Pro848Thr(p.P848T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000317276
Start	8142414:8142414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371070132
CDS Mutation	c.3304G>A
AA Mutation	p.Asp1102Asn(p.D1102N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000317276
Start	8143435:8143435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs3027193
CDS Mutation	c.2903G>A
AA Mutation	p.Arg968His(p.R968H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000317276
Start	8142673:8142673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3235G>A
AA Mutation	p.Gly1079Ser(p.G1079S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000317276
Start	8150684:8150684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.23C>A
AA Mutation	p.Ala8Asp(p.A8D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000317276
Start	8143783:8143783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778854573
CDS Mutation	c.2555C>T
AA Mutation	p.Ala852Val(p.A852V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000317276
Start	8142441:8142441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3277C>A
AA Mutation	p.His1093Asn(p.H1093N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317276
Start	8146058:8146058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773813301
CDS Mutation	c.2118C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317276
Start	8147286:8147286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146375404
CDS Mutation	c.1593C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317276
Start	8146469:8146469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1941T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317276
Start	8143761:8143761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2577C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317276
Start	8141257:8141257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3684G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000317276
Start	8147571:8147571(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs773913770
CDS Mutation	c.1396delC
AA Mutation	p.Leu466Ter(p.L466*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000317276
Start	8148093:8148093(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1138delC
AA Mutation	p.Leu380CysfsTer73(p.L380Cfs*73)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000317276
Start	8143454:8143454(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2884delG
AA Mutation	p.Ala962ProfsTer160(p.A962Pfs*160)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PER1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000317276
Start	8150662:8150662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.45G>T
AA Mutation	p.Arg15Ser(p.R15S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript