Colon Cancer: Gene >> VEGFC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000618562
Start	176683942:176683942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1244G>T
AA Mutation	p.Arg415Ile(p.R415I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000618562
Start	176729617:176729617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.277A>G
AA Mutation	p.Asn93Asp(p.N93D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000618562
Start	176683997:176683997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1189C>T
AA Mutation	p.Pro397Ser(p.P397S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000618562
Start	176729713:176729713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs566826535
CDS Mutation	c.181C>T
AA Mutation	p.Arg61Trp(p.R61W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000618562
Start	176687413:176687413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.919C>T
AA Mutation	p.His307Tyr(p.H307Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000618562
Start	176727891:176727891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745519188
CDS Mutation	c.439G>A
AA Mutation	p.Ala147Thr(p.A147T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000618562
Start	176684040:176684040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1146C>A
AA Mutation	p.Ser382Arg(p.S382R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000618562
Start	176687410:176687410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.922A>G
AA Mutation	p.Lys308Glu(p.K308E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000618562
Start	176727889:176727889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs560722685
CDS Mutation	c.441G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000618562
Start	176727856:176727856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778379951
CDS Mutation	c.474C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000618562
Start	176687432:176687432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.900G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000618562
Start	176687407:176687407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.925G>T
AA Mutation	p.Glu309Ter(p.E309*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000618562
Start	176727842:176727843(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.487_488insT
AA Mutation	p.Gly163ValfsTer6(p.G163Vfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> VEGFC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000618562
Start	176687848:176687848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.784T>G
AA Mutation	p.Phe262Val(p.F262V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000618562
Start	176729608:176729608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.286C>A
AA Mutation	p.Gln96Lys(p.Q96K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000618562
Start	176727890:176727890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.440C>T
AA Mutation	p.Ala147Val(p.A147V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000618562
Start	176729720:176729720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.174G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000618562
Start	176687854:176687854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.778G>T
AA Mutation	p.Glu260Ter(p.E260*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript