Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ARRDC3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265138
Start	91382956:91382956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.137C>A
AA Mutation	p.Ser46Tyr(p.S46Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265138
Start	91382947:91382947(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.146T>G
AA Mutation	p.Ile49Ser(p.I49S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265138
Start	91373794:91373794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1078A>G
AA Mutation	p.Asn360Asp(p.N360D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265138
Start	91375037:91375037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.755G>T
AA Mutation	p.Gly252Val(p.G252V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265138
Start	91374940:91374940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368267750
CDS Mutation	c.852C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265138
Start	91382921:91382922(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.171dupA
AA Mutation	p.Arg58ThrfsTer4(p.R58Tfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000265138
Start	91375179:91375179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.614-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> ARRDC3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265138
Start	91374167:91374167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.980A>G
AA Mutation	p.Gln327Arg(p.Q327R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265138
Start	91382890:91382890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.203A>C
AA Mutation	p.Asn68Thr(p.N68T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265138
Start	91382956:91382956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.137C>A
AA Mutation	p.Ser46Tyr(p.S46Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000265138
Start	91373713:91373713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1159C>T
AA Mutation	p.Arg387Ter(p.R387*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript