Colon Cancer: Gene >> PIK3R2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000222254
Start	18167162:18167162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1592G>A
AA Mutation	p.Arg531His(p.R531H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000222254
Start	18168776:18168776(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776438063
CDS Mutation	c.1859G>A
AA Mutation	p.Arg620His(p.R620H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000222254
Start	18160525:18160525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.377C>T
AA Mutation	p.Pro126Leu(p.P126L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000222254
Start	18163113:18163113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1256C>T
AA Mutation	p.Thr419Ile(p.T419I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000222254
Start	18163306:18163306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1334A>C
AA Mutation	p.Gln445Pro(p.Q445P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000222254
Start	18160548:18160548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.400G>A
AA Mutation	p.Ala134Thr(p.A134T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000222254
Start	18160942:18160942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768743781
CDS Mutation	c.439C>T
AA Mutation	p.Arg147Cys(p.R147C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000222254
Start	18163019:18163019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1162G>T
AA Mutation	p.Gly388Cys(p.G388C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222254
Start	18169222:18169222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2115C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000222254
Start	18160521:18160521(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.377delC
AA Mutation	p.Pro126LeufsTer4(p.P126Lfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000222254
Start	18160564:18160564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.415+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000222254
Start	18163042:18163044(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1187_1189delGCT
AA Mutation	p.Cys396del(p.C396del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PIK3R2

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222254
Start	18163078:18163078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762884959
CDS Mutation	c.1221C>T
Mutation Classification	Silent
Feature Type	Transcript