Colon Cancer: Gene >> PLA2G3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000215885
Start	31135871:31135871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150202365
CDS Mutation	c.1382G>A
AA Mutation	p.Arg461Gln(p.R461Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000215885
Start	31140017:31140017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.338G>T
AA Mutation	p.Ser113Ile(p.S113I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000215885
Start	31138712:31138712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199671180
CDS Mutation	c.602G>A
AA Mutation	p.Arg201Gln(p.R201Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000215885
Start	31138724:31138724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.590A>G
AA Mutation	p.Asn197Ser(p.N197S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000215885
Start	31138740:31138740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.574T>C
AA Mutation	p.Ser192Pro(p.S192P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000215885
Start	31136714:31136714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1285G>C
AA Mutation	p.Ala429Pro(p.A429P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000215885
Start	31138752:31138752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.562C>A
AA Mutation	p.Pro188Thr(p.P188T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000215885
Start	31140294:31140294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.61T>C
AA Mutation	p.Ser21Pro(p.S21P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000215885
Start	31140163:31140163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377694018
CDS Mutation	c.192G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000215885
Start	31140055:31140055(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs749116898
CDS Mutation	c.300delC
AA Mutation	p.Gly101AspfsTer252(p.G101Dfs*252)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000215885
Start	31140296:31140296(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.59delG
AA Mutation	p.Gly20AlafsTer14(p.G20Afs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PLA2G3

No Mutation Annotation!