Colon Cancer: Gene >> NRP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360409
Start	205745818:205745818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1714C>T
AA Mutation	p.Arg572Trp(p.R572W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000360409
Start	205794891:205794891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755038975
CDS Mutation	c.2629G>A
AA Mutation	p.Val877Ile(p.V877I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000360409
Start	205743361:205743361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762753258
CDS Mutation	c.1450G>A
AA Mutation	p.Gly484Ser(p.G484S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000360409
Start	205683316:205683316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.26T>C
AA Mutation	p.Val9Ala(p.V9A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000360409
Start	205743409:205743409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1498G>T
AA Mutation	p.Gly500Cys(p.G500C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000360409
Start	205792248:205792248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2454A>C
AA Mutation	p.Glu818Asp(p.E818D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000360409
Start	205794852:205794852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2590C>T
AA Mutation	p.Pro864Ser(p.P864S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000360409
Start	205726077:205726077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.985C>A
AA Mutation	p.Leu329Ile(p.L329I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000360409
Start	205752927:205752927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143177221
CDS Mutation	c.1996C>T
AA Mutation	p.Arg666Trp(p.R666W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000360409
Start	205765534:205765534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2368C>T
AA Mutation	p.Arg790Trp(p.R790W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000360409
Start	205763805:205763805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2176C>T
AA Mutation	p.Arg726Cys(p.R726C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000360409
Start	205716266:205716266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.325G>A
AA Mutation	p.Ala109Thr(p.A109T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360409
Start	205745751:205745751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748880896
CDS Mutation	c.1647C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360409
Start	205765482:205765482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752006505
CDS Mutation	c.2316C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360409
Start	205743393:205743393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1482A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360409
Start	205743237:205743237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1326A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360409
Start	205763756:205763756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2127G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360409
Start	205722515:205722515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs187188732
CDS Mutation	c.471C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000360409
Start	205763697:205763697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2068C>T
AA Mutation	p.Gln690Ter(p.Q690*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000360409
Start	205749751:205749751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1813G>T
AA Mutation	p.Gly605Ter(p.G605*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000360409
Start	205763690:205763691(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2061_2062insGTAT
AA Mutation	p.Arg688ValfsTer6(p.R688Vfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> NRP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360409
Start	205745887:205745887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1783A>G
AA Mutation	p.Thr595Ala(p.T595A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000360409
Start	205727928:205727928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1028C>A
AA Mutation	p.Ala343Glu(p.A343E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000360409
Start	205683300:205683300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.10T>C
AA Mutation	p.Phe4Leu(p.F4L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000360409
Start	205697657:205697657(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764826189
CDS Mutation	c.187G>A
AA Mutation	p.Glu63Lys(p.E63K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000360409
Start	205722540:205722540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.496C>A
AA Mutation	p.Pro166Thr(p.P166T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000360409
Start	205752876:205752876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150629453
CDS Mutation	c.1945G>A
AA Mutation	p.Asp649Asn(p.D649N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000360409
Start	205794830:205794830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2568G>T
AA Mutation	p.Lys856Asn(p.K856N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360409
Start	205743489:205743489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1578C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360409
Start	205752875:205752875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377534049
CDS Mutation	c.1944C>T
Mutation Classification	Silent
Feature Type	Transcript