Colon Cancer: Gene >> PHLPP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000568954
Start	71648898:71648898(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3964G>T
AA Mutation	p.Ala1322Ser(p.A1322S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000568954
Start	71649645:71649645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3217A>G
AA Mutation	p.Ser1073Gly(p.S1073G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000568954
Start	71679506:71679506(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.920C>T
AA Mutation	p.Ser307Phe(p.S307F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000568954
Start	71679466:71679466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.960G>T
AA Mutation	p.Glu320Asp(p.E320D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000568954
Start	71702667:71702667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.349G>C
AA Mutation	p.Asp117His(p.D117H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000568954
Start	71676485:71676485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1433G>T
AA Mutation	p.Ser478Ile(p.S478I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000568954
Start	71676470:71676470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1448G>A
AA Mutation	p.Arg483Gln(p.R483Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000568954
Start	71648958:71648958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760864609
CDS Mutation	c.3904C>T
AA Mutation	p.Arg1302Trp(p.R1302W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000568954
Start	71655249:71655249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2576T>C
AA Mutation	p.Val859Ala(p.V859A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000568954
Start	71648905:71648905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760184822
CDS Mutation	c.3957C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000568954
Start	71652856:71652856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2751C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000568954
Start	71652910:71652910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2697C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000568954
Start	71690564:71690564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.564T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000568954
Start	71653003:71653003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2604C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000568954
Start	71684595:71684595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.616G>T
AA Mutation	p.Glu206Ter(p.E206*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000568954
Start	71678758:71678758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1265T>G
AA Mutation	p.Leu422Ter(p.L422*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000568954
Start	71658296:71658297(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2215_2216insTAAGG
AA Mutation	p.Gln739LeufsTer7(p.Q739Lfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000568954
Start	71658364:71658364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2149-1G>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> PHLPP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000568954
Start	71656577:71656577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2384G>T
AA Mutation	p.Arg795Ile(p.R795I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000568954
Start	71658344:71658344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2168A>C
AA Mutation	p.Asn723Thr(p.N723T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000568954
Start	71658345:71658345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2167A>G
AA Mutation	p.Asn723Asp(p.N723D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000568954
Start	71652907:71652907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780474617
CDS Mutation	c.2700G>A
Mutation Classification	Silent
Feature Type	Transcript