Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> FLII

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000327031
Start	18245772:18245772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200966684
CDS Mutation	c.3475G>A
AA Mutation	p.Glu1159Lys(p.E1159K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000327031
Start	18253654:18253654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773795422
CDS Mutation	c.745C>T
AA Mutation	p.Arg249Cys(p.R249C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000327031
Start	18245191:18245191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs185087719
CDS Mutation	c.3757G>A
AA Mutation	p.Ala1253Thr(p.A1253T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000327031
Start	18245555:18245555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3609G>T
AA Mutation	p.Glu1203Asp(p.E1203D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000327031
Start	18247746:18247746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2398G>A
AA Mutation	p.Ala800Thr(p.A800T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000327031
Start	18245226:18245226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374452292
CDS Mutation	c.3722G>A
AA Mutation	p.Arg1241Gln(p.R1241Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000327031
Start	18246428:18246428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3086A>G
AA Mutation	p.Lys1029Arg(p.K1029R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000327031
Start	18246445:18246445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3069G>T
AA Mutation	p.Gln1023His(p.Q1023H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000327031
Start	18254585:18254585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.511C>T
AA Mutation	p.Arg171Cys(p.R171C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000327031
Start	18251768:18251768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1295G>A
AA Mutation	p.Arg432Lys(p.R432K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000327031
Start	18251772:18251772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1291C>T
AA Mutation	p.Arg431Trp(p.R431W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000327031
Start	18246627:18246627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3018G>C
AA Mutation	p.Lys1006Asn(p.K1006N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000327031
Start	18254563:18254563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140059134
CDS Mutation	c.533C>T
AA Mutation	p.Thr178Met(p.T178M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000327031
Start	18251291:18251291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1570G>A
AA Mutation	p.Glu524Lys(p.E524K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327031
Start	18256942:18256942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.141C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327031
Start	18247292:18247292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2553G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000327031
Start	18249178:18249178(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1883delA
AA Mutation	p.Lys628ArgfsTer27(p.K628Rfs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000327031
Start	18251454:18251454(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1407delC
AA Mutation	p.Ser470AlafsTer32(p.S470Afs*32)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> FLII

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000327031
Start	18246428:18246428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3086A>G
AA Mutation	p.Lys1029Arg(p.K1029R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000327031
Start	18245772:18245772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200966684
CDS Mutation	c.3475G>A
AA Mutation	p.Glu1159Lys(p.E1159K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000327031
Start	18251743:18251743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1320C>G
AA Mutation	p.Asp440Glu(p.D440E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript