Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> PRKAR1A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358598
Start	68522895:68522895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.317C>T
AA Mutation	p.Thr106Met(p.T106M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000358598
Start	68527889:68527889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.758T>C
AA Mutation	p.Val253Ala(p.V253A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358598
Start	68528937:68528937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.837G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358598
Start	68515462:68515462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777110464
CDS Mutation	c.63C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358598
Start	68525780:68525780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.576C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358598
Start	68529976:68529976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.948A>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PRKAR1A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358598
Start	68528897:68528897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.797C>A
AA Mutation	p.Thr266Lys(p.T266K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000358598
Start	68523737:68523737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.361G>T
AA Mutation	p.Asp121Tyr(p.D121Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000358598
Start	68530277:68530277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.974G>T
AA Mutation	p.Gly325Val(p.G325V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000358598
Start	68530406:68530406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1103G>A
AA Mutation	p.Arg368Gln(p.R368Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000358598
Start	68522888:68522888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.310G>A
AA Mutation	p.Val104Ile(p.V104I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript