Colon Cancer: Gene >> PML

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000268058
Start	73998248:73998248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.374C>T
AA Mutation	p.Ala125Val(p.A125V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000268058
Start	74044367:74044367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202099881
CDS Mutation	c.2008C>T
AA Mutation	p.Arg670Cys(p.R670C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000268058
Start	74023027:74023027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.802C>G
AA Mutation	p.Leu268Val(p.L268V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000268058
Start	73998139:73998139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.265C>A
AA Mutation	p.Pro89Thr(p.P89T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000268058
Start	74044562:74044562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2203G>A
AA Mutation	p.Ala735Thr(p.A735T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000268058
Start	74044260:74044260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1901G>T
AA Mutation	p.Ser634Ile(p.S634I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000268058
Start	73998232:73998232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141544943
CDS Mutation	c.358C>T
AA Mutation	p.Arg120Trp(p.R120W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000268058
Start	73998382:73998382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.508C>T
AA Mutation	p.Arg170Cys(p.R170C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000268058
Start	74044371:74044371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2012G>T
AA Mutation	p.Arg671Leu(p.R671L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000268058
Start	73998457:73998457(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.583C>T
AA Mutation	p.Arg195Cys(p.R195C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268058
Start	73998075:73998075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374118853
CDS Mutation	c.201G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268058
Start	74024903:74024903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1230C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268058
Start	74032598:74032598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1281C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268058
Start	74034485:74034485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139324287
CDS Mutation	c.1665C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268058
Start	74022855:74022855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767815962
CDS Mutation	c.630G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268058
Start	74044270:74044270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148185755
CDS Mutation	c.1911C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000268058
Start	73994885:73994885(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.78delC
AA Mutation	p.Glu27ArgfsTer71(p.E27Rfs*71)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000268058
Start	74023400:74023401(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1179dupG
AA Mutation	p.Lys394GlufsTer22(p.K394Efs*22)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> PML

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000268058
Start	74044811:74044811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2452G>A
AA Mutation	p.Gly818Arg(p.G818R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000268058
Start	73998215:73998215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.341G>A
AA Mutation	p.Arg114Gln(p.R114Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript