Colon Cancer: Gene >> PLEKHM2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375799
Start	15719789:15719789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.521A>G
AA Mutation	p.Tyr174Cys(p.Y174C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000375799
Start	15729800:15729800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2079C>A
AA Mutation	p.Phe693Leu(p.F693L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000375799
Start	15727799:15727799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1727G>A
AA Mutation	p.Ser576Asn(p.S576N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000375799
Start	15719900:15719900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373741350
CDS Mutation	c.632C>T
AA Mutation	p.Ala211Val(p.A211V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000375799
Start	15733902:15733902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781466914
CDS Mutation	c.3028C>T
AA Mutation	p.Arg1010Cys(p.R1010C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000375799
Start	15727477:15727477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748904369
CDS Mutation	c.1405G>A
AA Mutation	p.Val469Ile(p.V469I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000375799
Start	15725440:15725440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.836C>T
AA Mutation	p.Thr279Ile(p.T279I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000375799
Start	15727327:15727327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199522123
CDS Mutation	c.1255G>A
AA Mutation	p.Gly419Arg(p.G419R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000375799
Start	15727696:15727696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1624C>T
AA Mutation	p.Pro542Ser(p.P542S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000375799
Start	15725350:15725350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765918617
CDS Mutation	c.746G>A
AA Mutation	p.Arg249His(p.R249H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000375799
Start	15733845:15733845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201091991
CDS Mutation	c.2971T>C
AA Mutation	p.Phe991Leu(p.F991L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375799
Start	15725447:15725447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.843C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375799
Start	15730711:15730711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746130842
CDS Mutation	c.2388C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375799
Start	15727137:15727137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377142193
CDS Mutation	c.1065C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375799
Start	15731901:15731901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767988461
CDS Mutation	c.2478C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375799
Start	15733874:15733874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3000C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375799
Start	15727122:15727122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370961093
CDS Mutation	c.1050C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375799
Start	15731225:15731225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772926237
CDS Mutation	c.2433C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000375799
Start	15727184:15727184(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1117delC
AA Mutation	p.Gln373ArgfsTer22(p.Q373Rfs*22)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000375799
Start	15730622:15730622(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2304delC
AA Mutation	p.Glu769ArgfsTer51(p.E769Rfs*51)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000375799
Start	15727013:15727013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.942-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> PLEKHM2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375799
Start	15732642:15732642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2836C>T
AA Mutation	p.Pro946Ser(p.P946S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000375799
Start	15733847:15733847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2973C>A
AA Mutation	p.Phe991Leu(p.F991L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375799
Start	15733847:15733847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745838157
CDS Mutation	c.2973C>T
Mutation Classification	Silent
Feature Type	Transcript