Colon Cancer: Gene >> NEDD9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379446
Start	11189977:11189977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1892A>G
AA Mutation	p.Tyr631Cys(p.Y631C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000379446
Start	11190557:11190557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1312T>C
AA Mutation	p.Tyr438His(p.Y438H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000379446
Start	11190147:11190147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1722G>T
AA Mutation	p.Met574Ile(p.M574I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000379446
Start	11190468:11190468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1401G>T
AA Mutation	p.Lys467Asn(p.K467N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000379446
Start	11190923:11190923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.946G>A
AA Mutation	p.Ala316Thr(p.A316T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000379446
Start	11213366:11213366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775045232
CDS Mutation	c.374G>A
AA Mutation	p.Gly125Asp(p.G125D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000379446
Start	11185485:11185485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760782051
CDS Mutation	c.2182G>A
AA Mutation	p.Ala728Thr(p.A728T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000379446
Start	11185275:11185275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2392G>A
AA Mutation	p.Ala798Thr(p.A798T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000379446
Start	11213606:11213606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.134T>C
AA Mutation	p.Leu45Pro(p.L45P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000379446
Start	11185494:11185494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2173G>A
AA Mutation	p.Ala725Thr(p.A725T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000379446
Start	11191192:11191192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143747979
CDS Mutation	c.677C>T
AA Mutation	p.Pro226Leu(p.P226L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000379446
Start	11188258:11188258(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1955A>G
AA Mutation	p.Asn652Ser(p.N652S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000379446
Start	11213321:11213321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.419G>T
AA Mutation	p.Arg140Ile(p.R140I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000379446
Start	11191190:11191190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.679C>T
AA Mutation	p.Pro227Ser(p.P227S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379446
Start	11190813:11190813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs575153183
CDS Mutation	c.1056G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379446
Start	11190861:11190861(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1008A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379446
Start	11213284:11213284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.456A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379446
Start	11185612:11185612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376701334
CDS Mutation	c.2055G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379446
Start	11185315:11185315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200762899
CDS Mutation	c.2352C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379446
Start	11185339:11185339(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2328C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379446
Start	11185438:11185438(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2229G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000379446
Start	11191135:11191135(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.734delC
AA Mutation	p.Pro245LeufsTer3(p.P245Lfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000379446
Start	11213309:11213309(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs780429523
CDS Mutation	c.431delG
AA Mutation	p.Gly144GlufsTer11(p.G144Efs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> NEDD9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379446
Start	11190125:11190125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs41272545
CDS Mutation	c.1744G>A
AA Mutation	p.Gly582Ser(p.G582S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000379446
Start	11213673:11213673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753036528
CDS Mutation	c.67G>A
AA Mutation	p.Ala23Thr(p.A23T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000379446
Start	11185449:11185449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2218C>T
AA Mutation	p.Arg740Ter(p.R740*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript