Colon Cancer: Gene >> NRP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265371
Start	33213390:33213390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760427841
CDS Mutation	c.1610C>T
AA Mutation	p.Ala537Val(p.A537V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265371
Start	33270756:33270756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.349C>T
AA Mutation	p.Pro117Ser(p.P117S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265371
Start	33180176:33180176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2672G>T
AA Mutation	p.Arg891Ile(p.R891I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265371
Start	33186313:33186313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2238G>T
AA Mutation	p.Glu746Asp(p.E746D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265371
Start	33213574:33213574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs564902260
CDS Mutation	c.1426G>A
AA Mutation	p.Ala476Thr(p.A476T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265371
Start	33270834:33270834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs533652148
CDS Mutation	c.271G>A
AA Mutation	p.Asp91Asn(p.D91N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000265371
Start	33202949:33202949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1806A>C
AA Mutation	p.Glu602Asp(p.E602D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000265371
Start	33270750:33270750(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746144639
CDS Mutation	c.355C>A
AA Mutation	p.Leu119Ile(p.L119I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000265371
Start	33180165:33180165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2683G>T
AA Mutation	p.Ala895Ser(p.A895S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265371
Start	33263824:33263824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.480C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265371
Start	33330851:33330851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.105C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265371
Start	33270835:33270835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764061468
CDS Mutation	c.270C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265371
Start	33226188:33226188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs550303286
CDS Mutation	c.1083C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265371
Start	33270808:33270808(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.297delT
AA Mutation	p.Phe99LeufsTer9(p.F99Lfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000265371
Start	33254053:33254055(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.954_956delAGA
AA Mutation	p.Glu319del(p.E319del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> NRP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265371
Start	33213522:33213522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1478A>C
AA Mutation	p.Lys493Thr(p.K493T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265371
Start	33221836:33221836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1165G>T
AA Mutation	p.Asp389Tyr(p.D389Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265371
Start	33226144:33226144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769749073
CDS Mutation	c.1127A>G
AA Mutation	p.Asn376Ser(p.N376S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265371
Start	33226191:33226191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139187411
CDS Mutation	c.1080C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265371
Start	33185710:33185710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143858258
CDS Mutation	c.2349C>T
Mutation Classification	Silent
Feature Type	Transcript