Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> PRRG1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378628
Start	37453515:37453515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.551G>A
AA Mutation	p.Ser184Asn(p.S184N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000378628
Start	37453428:37453428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.464G>A
AA Mutation	p.Arg155His(p.R155H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000378628
Start	37425878:37425878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.49C>T
AA Mutation	p.Arg17Cys(p.R17C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000378628
Start	37453598:37453598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.634C>T
AA Mutation	p.Pro212Ser(p.P212S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378628
Start	37453222:37453222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.258G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000378628
Start	37453330:37453330(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.368delC
AA Mutation	p.Pro123LeufsTer30(p.P123Lfs*30)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PRRG1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378628
Start	37453479:37453479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.515A>T
AA Mutation	p.Tyr172Phe(p.Y172F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000378628
Start	37425952:37425952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.123C>A
AA Mutation	p.Phe41Leu(p.F41L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000378628
Start	37453449:37453449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782128331
CDS Mutation	c.485G>A
AA Mutation	p.Arg162His(p.R162H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378628
Start	37453228:37453228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.264C>A
Mutation Classification	Silent
Feature Type	Transcript