Colon Cancer: Gene >> CLIP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000223398
Start	74353989:74353989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.788C>T
AA Mutation	p.Ala263Val(p.A263V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000223398
Start	74376679:74376679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374499437
CDS Mutation	c.2278G>A
AA Mutation	p.Glu760Lys(p.E760K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000223398
Start	74360229:74360229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200008575
CDS Mutation	c.1270G>A
AA Mutation	p.Val424Met(p.V424M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000223398
Start	74380812:74380812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2428G>A
AA Mutation	p.Glu810Lys(p.E810K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000223398
Start	74357307:74357307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1045C>T
AA Mutation	p.Arg349Cys(p.R349C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000223398
Start	74317581:74317581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs151111065
CDS Mutation	c.35G>A
AA Mutation	p.Arg12His(p.R12H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000223398
Start	74372995:74372995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1444G>T
AA Mutation	p.Ala482Ser(p.A482S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000223398
Start	74357437:74357437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1175T>C
AA Mutation	p.Val392Ala(p.V392A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000223398
Start	74338708:74338708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.382C>T
AA Mutation	p.Arg128Cys(p.R128C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000223398
Start	74317577:74317577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200966015
CDS Mutation	c.31G>A
AA Mutation	p.Gly11Ser(p.G11S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000223398
Start	74360190:74360190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782384622
CDS Mutation	c.1231G>A
AA Mutation	p.Glu411Lys(p.E411K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000223398
Start	74376043:74376043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782208048
CDS Mutation	c.1642C>T
AA Mutation	p.Arg548Trp(p.R548W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000223398
Start	74400389:74400389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782670726
CDS Mutation	c.2900C>T
AA Mutation	p.Ser967Leu(p.S967L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000223398
Start	74317617:74317617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.71C>A
AA Mutation	p.Ser24Tyr(p.S24Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000223398
Start	74376638:74376638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767479757
CDS Mutation	c.2237C>T
AA Mutation	p.Ala746Val(p.A746V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000223398
Start	74376626:74376626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2225A>G
AA Mutation	p.Tyr742Cys(p.Y742C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000223398
Start	74357304:74357304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1042G>A
AA Mutation	p.Ala348Thr(p.A348T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000223398
Start	74389180:74389180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2641C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000223398
Start	74376075:74376075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1674G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000223398
Start	74356422:74356422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.816C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000223398
Start	74356593:74356593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199730295
CDS Mutation	c.987C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000223398
Start	74353918:74353918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.717G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000223398
Start	74353912:74353912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781970516
CDS Mutation	c.711C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000223398
Start	74356443:74356443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147879287
CDS Mutation	c.837C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000223398
Start	74380847:74380847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201362892
CDS Mutation	c.2463G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000223398
Start	74338590:74338590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs554341269
CDS Mutation	c.264C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000223398
Start	74338875:74338875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.549C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000223398
Start	74353915:74353915(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.718delG
AA Mutation	p.Glu240ArgfsTer46(p.E240Rfs*46)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000223398
Start	74317583:74317583(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.42delG
AA Mutation	p.Lys15SerfsTer73(p.K15Sfs*73)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CLIP2

No Mutation Annotation!