Colon Cancer: Gene >> PIK3C2A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265970
Start	17169027:17169027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.715A>C
AA Mutation	p.Asn239His(p.N239H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265970
Start	17169146:17169146(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.596C>A
AA Mutation	p.Pro199His(p.P199H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265970
Start	17169650:17169650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.92C>A
AA Mutation	p.Ala31Glu(p.A31E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265970
Start	17148764:17148764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1351A>G
AA Mutation	p.Ile451Val(p.I451V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265970
Start	17168885:17168885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.857T>C
AA Mutation	p.Val286Ala(p.V286A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265970
Start	17097115:17097115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755260229
CDS Mutation	c.4268G>A
AA Mutation	p.Arg1423Gln(p.R1423Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000265970
Start	17131989:17131989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2158C>A
AA Mutation	p.Leu720Ile(p.L720I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000265970
Start	17150539:17150539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1286A>G
AA Mutation	p.Asp429Gly(p.D429G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000265970
Start	17168997:17168997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.745A>G
AA Mutation	p.Thr249Ala(p.T249A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265970
Start	17169505:17169505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.237T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265970
Start	17102673:17102673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3840C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265970
Start	17122732:17122732(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2481delA
AA Mutation	p.Gly828AspfsTer7(p.G828Dfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000265970
Start	17105240:17105240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3610G>T
AA Mutation	p.Gly1204Ter(p.G1204*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000265970
Start	17136616:17136616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1714C>T
AA Mutation	p.Arg572Ter(p.R572*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained;frameshift_variant
Transcription ID	ENST00000265970
Start	17122269:17122270(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2575_2576insCTTGACTTTTACAT
AA Mutation	p.Ile859ThrfsTer2(p.I859Tfs*2)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265970
Start	17169162:17169163(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.579_580insTGCTTTC
AA Mutation	p.Pro194CysfsTer31(p.P194Cfs*31)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> PIK3C2A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265970
Start	17117538:17117538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3169G>C
AA Mutation	p.Gly1057Arg(p.G1057R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265970
Start	17169242:17169242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.500C>T
AA Mutation	p.Ala167Val(p.A167V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265970
Start	17099912:17099912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4066G>T
AA Mutation	p.Asp1356Tyr(p.D1356Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265970
Start	17091581:17091581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4718C>A
AA Mutation	p.Thr1573Asn(p.T1573N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265970
Start	17131948:17131948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2199G>T
AA Mutation	p.Lys733Asn(p.K733N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265970
Start	17118652:17118652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3028T>C
Mutation Classification	Silent
Feature Type	Transcript