Colon Cancer: Gene >> PLA2G2F

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375102
Start	20143523:20143523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.247T>C
AA Mutation	p.Ser83Pro(p.S83P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000375102
Start	20139509:20139509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202089729
CDS Mutation	c.82C>T
AA Mutation	p.Arg28Cys(p.R28C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375102
Start	20143498:20143498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139284980
CDS Mutation	c.222C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375102
Start	20144589:20144589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200119328
CDS Mutation	c.324C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375102
Start	20143553:20143553(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.277C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PLA2G2F

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375102
Start	20140209:20140209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.160G>A
AA Mutation	p.Ala54Thr(p.A54T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000375102
Start	20143563:20143563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145617803
CDS Mutation	c.287G>A
AA Mutation	p.Arg96His(p.R96H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375102
Start	20148398:20148398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.633C>A
Mutation Classification	Silent
Feature Type	Transcript