Colon Cancer: Gene >> PIK3R5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000447110
Start	8889181:8889181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.853G>A
AA Mutation	p.Val285Ile(p.V285I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000447110
Start	8887131:8887131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1870G>A
AA Mutation	p.Gly624Ser(p.G624S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000447110
Start	8888294:8888294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765654812
CDS Mutation	c.1493G>A
AA Mutation	p.Arg498His(p.R498H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000447110
Start	8888280:8888280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772438975
CDS Mutation	c.1507C>T
AA Mutation	p.Arg503Cys(p.R503C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000447110
Start	8893599:8893599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775978234
CDS Mutation	c.469C>T
AA Mutation	p.Arg157Cys(p.R157C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000447110
Start	8893650:8893650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.418T>G
AA Mutation	p.Ser140Ala(p.S140A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000447110
Start	8888424:8888424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757235159
CDS Mutation	c.1363C>T
AA Mutation	p.Arg455Trp(p.R455W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000447110
Start	8887666:8887666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760651514
CDS Mutation	c.1634G>A
AA Mutation	p.Arg545His(p.R545H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000447110
Start	8887143:8887143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1858C>T
AA Mutation	p.Arg620Cys(p.R620C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000447110
Start	8888171:8888171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1616G>A
AA Mutation	p.Arg539Gln(p.R539Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000447110
Start	8880702:8880702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2580C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000447110
Start	8904841:8904841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.348T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000447110
Start	8893624:8893624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.444G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000447110
Start	8884731:8884731(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2181A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000447110
Start	8905703:8905703(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.239delC
AA Mutation	p.Pro80ArgfsTer24(p.P80Rfs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000447110
Start	8887202:8887203(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1798dupT
AA Mutation	p.Trp600LeufsTer7(p.W600Lfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> PIK3R5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000447110
Start	8881865:8881865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2222G>A
AA Mutation	p.Arg741Gln(p.R741Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000447110
Start	8890843:8890843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.552G>A
Mutation Classification	Silent
Feature Type	Transcript