Colon Cancer: Gene >> PIK3C3

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000262039
Start	42037693:42037693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1841G>A
AA Mutation	p.Ser614Asn(p.S614N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262039
Start	42029331:42029331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1597A>G
AA Mutation	p.Lys533Glu(p.K533E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262039
Start	42004480:42004480(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1109A>G
AA Mutation	p.His370Arg(p.H370R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262039
Start	41962614:41962614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200002230
CDS Mutation	c.383C>T
AA Mutation	p.Ser128Leu(p.S128L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262039
Start	41957628:41957628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.127A>C
AA Mutation	p.Met43Leu(p.M43L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262039
Start	41962551:41962551(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.320C>T
AA Mutation	p.Ala107Val(p.A107V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000262039
Start	42013489:42013489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1218A>T
AA Mutation	p.Glu406Asp(p.E406D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262039
Start	42067402:42067402(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2538C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262039
Start	41957663:41957663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.162C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262039
Start	42058031:42058031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2412G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262039
Start	42033945:42033945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1827T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262039
Start	42037733:42037733(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1881T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262039
Start	42037716:42037716(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1869delT
AA Mutation	p.Phe623LeufsTer43(p.F623Lfs*43)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262039
Start	41993326:41993326(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.775delC
AA Mutation	p.Gln259ArgfsTer7(p.Q259Rfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PIK3C3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262039
Start	42004370:42004370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200744647
CDS Mutation	c.999C>A
AA Mutation	p.Phe333Leu(p.F333L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262039
Start	42015483:42015483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1333A>C
AA Mutation	p.Ile445Leu(p.I445L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000262039
Start	41987878:41987878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.598G>T
AA Mutation	p.Glu200Ter(p.E200*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript