Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> PRKRA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000325748
Start	178432210:178432210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.829T>A
AA Mutation	p.Ser277Thr(p.S277T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000325748
Start	178432118:178432118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.921G>T
AA Mutation	p.Lys307Asn(p.K307N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000325748
Start	178444452:178444452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765454211
CDS Mutation	c.366G>T
AA Mutation	p.Lys122Asn(p.K122N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000325748
Start	178450320:178450320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.157G>A
AA Mutation	p.Glu53Lys(p.E53K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000325748
Start	178443335:178443335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.446A>G
AA Mutation	p.Gln149Arg(p.Q149R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000325748
Start	178450386:178450386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.91C>T
AA Mutation	p.Pro31Ser(p.P31S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000325748
Start	178432129:178432129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.910C>T
AA Mutation	p.Gln304Ter(p.Q304*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PRKRA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000325748
Start	178441689:178441689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.530A>C
AA Mutation	p.Lys177Thr(p.K177T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000325748
Start	178432179:178432179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.860C>T
AA Mutation	p.Ser287Phe(p.S287F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000325748
Start	178444452:178444452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765454211
CDS Mutation	c.366G>T
AA Mutation	p.Lys122Asn(p.K122N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript