Colon Cancer: Gene >> MPRIP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000341712
Start	17158832:17158832(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768965649
CDS Mutation	c.1876G>A
AA Mutation	p.Asp626Asn(p.D626N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000341712
Start	17154331:17154331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1391C>T
AA Mutation	p.Ser464Leu(p.S464L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000341712
Start	17142749:17142749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777364536
CDS Mutation	c.1019C>T
AA Mutation	p.Ala340Val(p.A340V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000341712
Start	17136321:17136321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.607C>G
AA Mutation	p.Leu203Val(p.L203V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000341712
Start	17158490:17158490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs555403048
CDS Mutation	c.1534A>G
AA Mutation	p.Thr512Ala(p.T512A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000341712
Start	17126769:17126769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.335G>A
AA Mutation	p.Arg112His(p.R112H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000341712
Start	17078024:17078024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.215G>A
AA Mutation	p.Arg72Gln(p.R72Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000341712
Start	17161337:17161337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763818544
CDS Mutation	c.2144G>A
AA Mutation	p.Arg715His(p.R715H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000341712
Start	17158961:17158961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765177491
CDS Mutation	c.2005C>T
AA Mutation	p.Arg669Trp(p.R669W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000341712
Start	17126706:17126706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.272C>T
AA Mutation	p.Thr91Met(p.T91M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000341712
Start	17158925:17158925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141452605
CDS Mutation	c.1969G>A
AA Mutation	p.Ala657Thr(p.A657T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000341712
Start	17137940:17137940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753280493
CDS Mutation	c.761G>A
AA Mutation	p.Arg254His(p.R254H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000341712
Start	17158596:17158596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1640A>G
AA Mutation	p.Glu547Gly(p.E547G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341712
Start	17177306:17177306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762579889
CDS Mutation	c.2853G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341712
Start	17154392:17154392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755779604
CDS Mutation	c.1452G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341712
Start	17175337:17175337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2634G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341712
Start	17143594:17143594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764009264
CDS Mutation	c.1074C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341712
Start	17126806:17126806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.372T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000341712
Start	17143605:17143605(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1090delC
AA Mutation	p.Leu364CysfsTer19(p.L364Cfs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000341712
Start	17143572:17143572(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1058delC
AA Mutation	p.Pro353GlnfsTer30(p.P353Qfs*30)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000341712
Start	17158446:17158446(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1496delA
AA Mutation	p.Asn499ThrfsTer126(p.N499Tfs*126)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000341712
Start	17147389:17147389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1275+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> MPRIP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000341712
Start	17158555:17158555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1599G>T
AA Mutation	p.Glu533Asp(p.E533D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript