Colon Cancer: Gene >> PLA2G15

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000219345
Start	68259377:68259377(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777652754
CDS Mutation	c.959C>T
AA Mutation	p.Ala320Val(p.A320V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000219345
Start	68255829:68255829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.566G>A
AA Mutation	p.Gly189Glu(p.G189E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000219345
Start	68249379:68249379(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.217T>C
AA Mutation	p.Phe73Leu(p.F73L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000219345
Start	68259637:68259637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1219C>T
AA Mutation	p.Arg407Cys(p.R407C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219345
Start	68255346:68255346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.468C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219345
Start	68259228:68259228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.810G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000219345
Start	68255952:68255952(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.695delG
AA Mutation	p.Gly232AlafsTer23(p.G232Afs*23)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000219345
Start	68255951:68255952(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs763871300
CDS Mutation	c.695dupG
AA Mutation	p.Val233ArgfsTer47(p.V233Rfs*47)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> PLA2G15

No Mutation Annotation!