Colon Cancer: Gene >> TIE1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372476
Start	43311790:43311790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757030245
CDS Mutation	c.1453C>T
AA Mutation	p.Arg485Trp(p.R485W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000372476
Start	43313275:43313275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2068C>T
AA Mutation	p.Pro690Ser(p.P690S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000372476
Start	43318028:43318028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755542003
CDS Mutation	c.2878G>A
AA Mutation	p.Ala960Thr(p.A960T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000372476
Start	43321404:43321404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3157C>T
AA Mutation	p.Pro1053Ser(p.P1053S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000372476
Start	43313344:43313344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780808450
CDS Mutation	c.2137C>T
AA Mutation	p.Arg713Cys(p.R713C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000372476
Start	43312451:43312451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144699870
CDS Mutation	c.1777C>T
AA Mutation	p.Arg593Trp(p.R593W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000372476
Start	43305063:43305063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767336788
CDS Mutation	c.271C>T
AA Mutation	p.Arg91Cys(p.R91C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000372476
Start	43306857:43306857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.502C>A
AA Mutation	p.Leu168Met(p.L168M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000372476
Start	43311746:43311746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140190628
CDS Mutation	c.1409C>T
AA Mutation	p.Ser470Leu(p.S470L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000372476
Start	43312487:43312487(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1813G>A
AA Mutation	p.Ala605Thr(p.A605T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000372476
Start	43305147:43305147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.355G>A
AA Mutation	p.Val119Met(p.V119M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000372476
Start	43305130:43305130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.338G>A
AA Mutation	p.Arg113His(p.R113H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000372476
Start	43313312:43313312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2105G>T
AA Mutation	p.Ser702Ile(p.S702I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000372476
Start	43321470:43321470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3223C>T
AA Mutation	p.Pro1075Ser(p.P1075S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372476
Start	43305107:43305107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.315C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372476
Start	43307806:43307806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.924T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372476
Start	43309495:43309495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754628532
CDS Mutation	c.1296C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372476
Start	43311747:43311747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770765264
CDS Mutation	c.1410G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372476
Start	43305315:43305315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.456G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372476
Start	43312375:43312375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1701C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372476
Start	43313334:43313334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2127C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372476
Start	43322689:43322689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773113655
CDS Mutation	c.3384C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000372476
Start	43307239:43307239(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.743delC
AA Mutation	p.Pro248LeufsTer117(p.P248Lfs*117)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000372476
Start	43313144:43313144(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1942delC
AA Mutation	p.Arg648AspfsTer15(p.R648Dfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000372476
Start	43321662:43321662(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3297delC
AA Mutation	p.Phe1100LeufsTer8(p.F1100Lfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TIE1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372476
Start	43321476:43321476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3229A>G
AA Mutation	p.Asn1077Asp(p.N1077D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000372476
Start	43321474:43321474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371464988
CDS Mutation	c.3227G>A
AA Mutation	p.Arg1076Gln(p.R1076Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372476
Start	43312432:43312432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201759080
CDS Mutation	c.1758C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372476
Start	43322689:43322689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773113655
CDS Mutation	c.3384C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000372476
Start	43318057:43318057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2907C>A
AA Mutation	p.Tyr969Ter(p.Y969*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript