Colon Cancer: Gene >> CLIP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000540338
Start	122341424:122341424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780769680
CDS Mutation	c.1780G>A
AA Mutation	p.Ala594Thr(p.A594T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000540338
Start	122341653:122341653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1551A>T
AA Mutation	p.Lys517Asn(p.K517N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000540338
Start	122347454:122347454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1427G>A
AA Mutation	p.Arg476His(p.R476H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000540338
Start	122377495:122377495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs113784516
CDS Mutation	c.551C>T
AA Mutation	p.Pro184Leu(p.P184L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000540338
Start	122279043:122279043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3750G>T
AA Mutation	p.Glu1250Asp(p.E1250D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000540338
Start	122364080:122364080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.685C>T
AA Mutation	p.Arg229Trp(p.R229W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000540338
Start	122341465:122341465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1739G>A
AA Mutation	p.Arg580Gln(p.R580Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000540338
Start	122272946:122272946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4246C>T
AA Mutation	p.Arg1416Cys(p.R1416C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000540338
Start	122273065:122273065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4127G>A
AA Mutation	p.Arg1376His(p.R1376H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000540338
Start	122272945:122272945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4247G>A
AA Mutation	p.Arg1416His(p.R1416H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000540338
Start	122377696:122377696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.350T>C
AA Mutation	p.Ile117Thr(p.I117T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000540338
Start	122319233:122319233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3365A>G
AA Mutation	p.Glu1122Gly(p.E1122G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000540338
Start	122340771:122340771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2433G>T
AA Mutation	p.Lys811Asn(p.K811N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000540338
Start	122341466:122341466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767835144
CDS Mutation	c.1738C>T
AA Mutation	p.Arg580Trp(p.R580W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000540338
Start	122319335:122319335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3263C>T
AA Mutation	p.Ala1088Val(p.A1088V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000540338
Start	122377477:122377477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.569A>C
AA Mutation	p.Lys190Thr(p.K190T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000540338
Start	122377602:122377602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.444G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000540338
Start	122327959:122327959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145339976
CDS Mutation	c.3237C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000540338
Start	122355127:122355127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146982254
CDS Mutation	c.1191C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000540338
Start	122279124:122279124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756613341
CDS Mutation	c.3669C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000540338
Start	122377727:122377727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.319C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000540338
Start	122380372:122380372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138117323
CDS Mutation	c.81G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000540338
Start	122336722:122336722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773264545
CDS Mutation	c.2478G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000540338
Start	122340849:122340849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2355A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000540338
Start	122328315:122328321(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2973_2979delAGAAGCA
AA Mutation	p.Glu992LeufsTer32(p.E992Lfs*32)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000540338
Start	122288490:122288490(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs761972338
CDS Mutation	c.3646delA
AA Mutation	p.Arg1216GlufsTer6(p.R1216Efs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000540338
Start	122316771:122316771(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3451delA
AA Mutation	p.Met1151TrpfsTer8(p.M1151Wfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	stop_gained
Transcription ID	ENST00000540338
Start	122316753:122316753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3469G>T
AA Mutation	p.Glu1157Ter(p.E1157*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	stop_gained
Transcription ID	ENST00000540338
Start	122341181:122341181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2023G>T
AA Mutation	p.Glu675Ter(p.E675*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000540338
Start	122319349:122319349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3250-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> CLIP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000540338
Start	122309782:122309782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756842406
CDS Mutation	c.3574G>A
AA Mutation	p.Glu1192Lys(p.E1192K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000540338
Start	122278919:122278919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148653401
CDS Mutation	c.3789C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000540338
Start	122341218:122341218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1986A>G
Mutation Classification	Silent
Feature Type	Transcript