Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> RAD9B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000392672
Start	110515134:110515134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.573G>T
AA Mutation	p.Lys191Asn(p.K191N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000392672
Start	110522410:110522410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1124A>C
AA Mutation	p.Lys375Thr(p.K375T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000392672
Start	110506666:110506666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.361G>T
AA Mutation	p.Val121Leu(p.V121L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000392672
Start	110506588:110506588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.283C>T
AA Mutation	p.Pro95Ser(p.P95S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392672
Start	110505743:110505743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.244C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000392672
Start	110503868:110503868(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.114delA
AA Mutation	p.Gly39ValfsTer4(p.G39Vfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000392672
Start	110522190:110522191(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.911dupA
AA Mutation	p.Ala305GlyfsTer25(p.A305Gfs*25)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> RAD9B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000392672
Start	110512788:110512788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753006923
CDS Mutation	c.398G>T
AA Mutation	p.Arg133Ile(p.R133I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000392672
Start	110518731:110518731(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.651C>A
AA Mutation	p.Phe217Leu(p.F217L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000392672
Start	110531588:110531588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762718499
CDS Mutation	c.1249G>T
AA Mutation	p.Glu417Ter(p.E417*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript