Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> RRH

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000317735
Start	109833235:109833235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.203C>T
AA Mutation	p.Ala68Val(p.A68V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000317735
Start	109833207:109833207(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.175C>T
AA Mutation	p.Pro59Ser(p.P59S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000317735
Start	109833172:109833172(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.140T>C
AA Mutation	p.Leu47Pro(p.L47P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000317735
Start	109842562:109842562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.814C>A
AA Mutation	p.Pro272Thr(p.P272T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317735
Start	109837530:109837530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.645C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained;frameshift_variant
Transcription ID	ENST00000317735
Start	109836152:109836153(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.543_544insTATTAGC
AA Mutation	p.Asn182TyrfsTer2(p.N182Yfs*2)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> RRH

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000317735
Start	109844190:109844190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1007G>T
AA Mutation	p.Arg336Ile(p.R336I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000317735
Start	109828035:109828035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.8G>T
AA Mutation	p.Arg3Ile(p.R3I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000317735
Start	109833307:109833307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.275A>C
AA Mutation	p.Lys92Thr(p.K92T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000317735
Start	109842604:109842604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.856T>G
AA Mutation	p.Ser286Ala(p.S286A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript