Colon Cancer: Gene >> PHLPP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262719
Start	62978991:62978991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4714A>C
AA Mutation	p.Ser1572Arg(p.S1572R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262719
Start	62895022:62895022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2078T>C
AA Mutation	p.Leu693Ser(p.L693S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262719
Start	62895870:62895870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2303C>A
AA Mutation	p.Ser768Tyr(p.S768Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262719
Start	62978778:62978778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763806257
CDS Mutation	c.4501G>A
AA Mutation	p.Gly1501Arg(p.G1501R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262719
Start	62963417:62963417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3505G>A
AA Mutation	p.Gly1169Arg(p.G1169R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262719
Start	62975543:62975543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3902C>T
AA Mutation	p.Pro1301Leu(p.P1301L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000262719
Start	62979204:62979204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4927G>A
AA Mutation	p.Ala1643Thr(p.A1643T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000262719
Start	62978998:62978998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4721C>T
AA Mutation	p.Ala1574Val(p.A1574V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000262719
Start	62978790:62978790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4513G>A
AA Mutation	p.Glu1505Lys(p.E1505K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000262719
Start	62972591:62972591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3638G>A
AA Mutation	p.Arg1213Gln(p.R1213Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000262719
Start	62895951:62895951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746842120
CDS Mutation	c.2384T>C
AA Mutation	p.Val795Ala(p.V795A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000262719
Start	62978381:62978381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4104C>A
AA Mutation	p.Phe1368Leu(p.F1368L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000262719
Start	62963457:62963457(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757930377
CDS Mutation	c.3545C>T
AA Mutation	p.Ser1182Leu(p.S1182L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000262719
Start	62978479:62978479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4202A>G
AA Mutation	p.Lys1401Arg(p.K1401R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262719
Start	62903159:62903159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2640T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262719
Start	62978798:62978798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4521C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262719
Start	62978789:62978789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750341239
CDS Mutation	c.4512C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262719
Start	62963464:62963464(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3557delA
AA Mutation	p.Asn1186ThrfsTer10(p.N1186Tfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000262719
Start	62895123:62895123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776883345
CDS Mutation	c.2179C>T
AA Mutation	p.Arg727Ter(p.R727*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000262719
Start	62945263:62945263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3316G>T
AA Mutation	p.Glu1106Ter(p.E1106*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262719
Start	62972653:62972654(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.3706dupA
AA Mutation	p.Thr1236AsnfsTer38(p.T1236Nfs*38)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	inframe_deletion;splice_region_variant
Transcription ID	ENST00000262719
Start	62838786:62838788(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1781_1783delAAG
AA Mutation	p.Glu594del(p.E594del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PHLPP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262719
Start	62895054:62895054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2110G>C
AA Mutation	p.Gly704Arg(p.G704R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262719
Start	62978855:62978855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4578C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262719
Start	62979090:62979090(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.4814delG
AA Mutation	p.Gly1605ValfsTer32(p.G1605Vfs*32)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000262719
Start	62975530:62975530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3889C>T
AA Mutation	p.Arg1297Ter(p.R1297*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript