Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ADCYAP1R1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000304166
Start	31064891:31064891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.112A>G
AA Mutation	p.Ile38Val(p.I38V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000304166
Start	31092653:31092653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.964G>T
AA Mutation	p.Val322Leu(p.V322L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000304166
Start	31085326:31085326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.553C>T
AA Mutation	p.Arg185Cys(p.R185C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000304166
Start	31103277:31103277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1087G>A
AA Mutation	p.Gly363Arg(p.G363R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000304166
Start	31084144:31084144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761532830
CDS Mutation	c.332T>C
AA Mutation	p.Met111Thr(p.M111T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304166
Start	31086497:31086497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.783T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ADCYAP1R1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000304166
Start	31106605:31106605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1328G>T
AA Mutation	p.Gly443Val(p.G443V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000304166
Start	31064879:31064879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.100T>C
AA Mutation	p.Cys34Arg(p.C34R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000304166
Start	31106588:31106588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1311C>A
AA Mutation	p.Ser437Arg(p.S437R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304166
Start	31092715:31092715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1026C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304166
Start	31084169:31084169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375886816
CDS Mutation	c.357G>A
Mutation Classification	Silent
Feature Type	Transcript