Colon Cancer: Gene >> PPRC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000278070
Start	102140264:102140264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1756C>T
AA Mutation	p.Pro586Ser(p.P586S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000278070
Start	102140796:102140796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777850442
CDS Mutation	c.2288G>A
AA Mutation	p.Arg763His(p.R763H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000278070
Start	102139236:102139236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.728G>A
AA Mutation	p.Arg243His(p.R243H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000278070
Start	102140933:102140933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2425A>G
AA Mutation	p.Arg809Gly(p.R809G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000278070
Start	102137889:102137889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.193A>G
AA Mutation	p.Ser65Gly(p.S65G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000278070
Start	102140639:102140639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs17847386
CDS Mutation	c.2131G>A
AA Mutation	p.Val711Met(p.V711M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000278070
Start	102148888:102148888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4689C>A
AA Mutation	p.Phe1563Leu(p.F1563L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000278070
Start	102149224:102149224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4786G>A
AA Mutation	p.Ala1596Thr(p.A1596T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000278070
Start	102141449:102141449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2941C>T
AA Mutation	p.Pro981Ser(p.P981S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000278070
Start	102138918:102138918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771663512
CDS Mutation	c.529C>T
AA Mutation	p.Arg177Cys(p.R177C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000278070
Start	102147389:102147389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749450563
CDS Mutation	c.4397G>A
AA Mutation	p.Arg1466Gln(p.R1466Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000278070
Start	102139230:102139230(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.722A>C
AA Mutation	p.Gln241Pro(p.Q241P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000278070
Start	102140301:102140301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1793G>A
AA Mutation	p.Gly598Asp(p.G598D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000278070
Start	102140784:102140784(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2276G>A
AA Mutation	p.Arg759Gln(p.R759Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000278070
Start	102149203:102149203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4765C>T
AA Mutation	p.Arg1589Cys(p.R1589C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000278070
Start	102140795:102140795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs542386144
CDS Mutation	c.2287C>T
AA Mutation	p.Arg763Cys(p.R763C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000278070
Start	102143078:102143078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3530A>G
AA Mutation	p.Glu1177Gly(p.E1177G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000278070
Start	102141705:102141705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144417602
CDS Mutation	c.3197C>T
AA Mutation	p.Pro1066Leu(p.P1066L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278070
Start	102138654:102138654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.378G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278070
Start	102141523:102141523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3015C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278070
Start	102139816:102139816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749670501
CDS Mutation	c.1308G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278070
Start	102139333:102139333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.825C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278070
Start	102149250:102149250(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4812G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278070
Start	102141148:102141148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760655362
CDS Mutation	c.2640T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278070
Start	102140077:102140077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1569T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000278070
Start	102140614:102140614(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2111delG
AA Mutation	p.Gly704ValfsTer30(p.G704Vfs*30)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	stop_gained
Transcription ID	ENST00000278070
Start	102148400:102148400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4429C>T
AA Mutation	p.Arg1477Ter(p.R1477*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	stop_gained
Transcription ID	ENST00000278070
Start	102147388:102147388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4396C>T
AA Mutation	p.Arg1466Ter(p.R1466*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PPRC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000278070
Start	102133175:102133175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.107G>A
AA Mutation	p.Ser36Asn(p.S36N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000278070
Start	102141606:102141606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761599601
CDS Mutation	c.3098C>T
AA Mutation	p.Ser1033Leu(p.S1033L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000278070
Start	102139878:102139878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1370G>A
AA Mutation	p.Arg457Gln(p.R457Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278070
Start	102139558:102139558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1050G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000278070
Start	102140290:102140291(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1783dupA
AA Mutation	p.Thr595AsnfsTer14(p.T595Nfs*14)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript