Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ODF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000434106
Start	128484034:128484034(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1084C>T
AA Mutation	p.Arg362Cys(p.R362C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000434106
Start	128469298:128469298(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs35903554
CDS Mutation	c.365G>A
AA Mutation	p.Arg122His(p.R122H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000434106
Start	128494643:128494643(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1886C>T
AA Mutation	p.Ala629Val(p.A629V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000434106
Start	128494599:128494599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1842A>T
AA Mutation	p.Gln614His(p.Q614H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000434106
Start	128498424:128498424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749830728
CDS Mutation	c.2024C>T
AA Mutation	p.Ala675Val(p.A675V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000434106
Start	128500178:128500178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372276840
CDS Mutation	c.2413G>A
AA Mutation	p.Ala805Thr(p.A805T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000434106
Start	128484845:128484845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1249G>A
AA Mutation	p.Glu417Lys(p.E417K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000434106
Start	128500070:128500070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2305G>A
AA Mutation	p.Asp769Asn(p.D769N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000434106
Start	128484847:128484847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1251G>T
AA Mutation	p.Glu417Asp(p.E417D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000434106
Start	128471388:128471388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.501C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000434106
Start	128459600:128459600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.66T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000434106
Start	128492716:128492716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1663T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000434106
Start	128469212:128469212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.279A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000434106
Start	128461023:128461023(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.209delC
AA Mutation	p.Pro70LeufsTer33(p.P70Lfs*33)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000434106
Start	128500204:128500204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2439T>A
AA Mutation	p.Tyr813Ter(p.Y813*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000434106
Start	128484830:128484830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1234C>T
AA Mutation	p.Arg412Ter(p.R412*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000434106
Start	128469203:128469204(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.270_271insGCTT
AA Mutation	p.Ile91AlafsTer18(p.I91Afs*18)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ODF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000434106
Start	128500206:128500206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2441C>A
AA Mutation	p.Ser814Tyr(p.S814Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000434106
Start	128459637:128459637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143901110
CDS Mutation	c.103G>A
AA Mutation	p.Ala35Thr(p.A35T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000434106
Start	128500227:128500227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2462C>G
AA Mutation	p.Pro821Arg(p.P821R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000434106
Start	128469302:128469302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.369T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000434106
Start	128471418:128471418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767852970
CDS Mutation	c.531G>A
Mutation Classification	Silent
Feature Type	Transcript