Colon Cancer: Gene >> PLA2G6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000332509
Start	38128334:38128334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1283C>T
AA Mutation	p.Ala428Val(p.A428V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000332509
Start	38132871:38132871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772176591
CDS Mutation	c.1037G>A
AA Mutation	p.Arg346His(p.R346H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000332509
Start	38140147:38140147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.632C>T
AA Mutation	p.Ala211Val(p.A211V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000332509
Start	38113554:38113554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2135G>A
AA Mutation	p.Ser712Asn(p.S712N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000332509
Start	38115531:38115531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369038599
CDS Mutation	c.2030G>A
AA Mutation	p.Arg677His(p.R677H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000332509
Start	38169245:38169245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780605573
CDS Mutation	c.182A>G
AA Mutation	p.Asn61Ser(p.N61S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000332509
Start	38129540:38129540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1100A>C
AA Mutation	p.Lys367Thr(p.K367T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000332509
Start	38143193:38143193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.521A>T
AA Mutation	p.Tyr174Phe(p.Y174F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000332509
Start	38128289:38128289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375740918
CDS Mutation	c.1328C>T
AA Mutation	p.Pro443Leu(p.P443L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000332509
Start	38126371:38126371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146684391
CDS Mutation	c.1427C>T
AA Mutation	p.Thr476Ile(p.T476I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000332509
Start	38116127:38116127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1827G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000332509
Start	38116094:38116094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1860G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000332509
Start	38113545:38113545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2144G>A
AA Mutation	p.Trp715Ter(p.W715*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000332509
Start	38128431:38128431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1187-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> PLA2G6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000332509
Start	38132937:38132937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757139688
CDS Mutation	c.971C>T
AA Mutation	p.Ala324Val(p.A324V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript