Colon Cancer: Gene >> PLA2G7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000274793
Start	46710561:46710561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.761A>G
AA Mutation	p.Asp254Gly(p.D254G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000274793
Start	46716489:46716489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.271G>A
AA Mutation	p.Asp91Asn(p.D91N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000274793
Start	46711506:46711506(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201567357
CDS Mutation	c.653G>A
AA Mutation	p.Arg218Gln(p.R218Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000274793
Start	46716429:46716429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.331C>A
AA Mutation	p.Leu111Ile(p.L111I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000274793
Start	46705203:46705203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1139C>A
AA Mutation	p.Ala380Asp(p.A380D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000274793
Start	46708147:46708147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.884T>C
AA Mutation	p.Leu295Pro(p.L295P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000274793
Start	46710584:46710584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.738G>T
AA Mutation	p.Lys246Asn(p.K246N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000274793
Start	46709397:46709397(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.799delA
AA Mutation	p.Ile267Ter(p.I267*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PLA2G7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000274793
Start	46704607:46704607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1279C>A
AA Mutation	p.Gln427Lys(p.Q427K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000274793
Start	46708043:46708043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.988A>C
AA Mutation	p.Lys330Gln(p.K330Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript