Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ARIH1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379887
Start	72580857:72580857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1342C>T
AA Mutation	p.His448Tyr(p.H448Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000379887
Start	72563495:72563495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.906A>C
AA Mutation	p.Gln302His(p.Q302H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000379887
Start	72572152:72572152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1202G>A
AA Mutation	p.Arg401Lys(p.R401K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000379887
Start	72563475:72563475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.886C>T
AA Mutation	p.Arg296Cys(p.R296C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ARIH1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379887
Start	72563475:72563475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.886C>T
AA Mutation	p.Arg296Cys(p.R296C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000379887
Start	72474911:72474911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.272C>T
AA Mutation	p.Pro91Leu(p.P91L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000379887
Start	72555301:72555301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.619T>C
AA Mutation	p.Phe207Leu(p.F207L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000379887
Start	72561536:72561536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.791A>C
AA Mutation	p.Asn264Thr(p.N264T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript