Colon Cancer: Gene >> SEMA4A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000355014
Start	156176941:156176941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2230A>G
AA Mutation	p.Thr744Ala(p.T744A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000355014
Start	156158107:156158107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.338G>A
AA Mutation	p.Cys113Tyr(p.C113Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000355014
Start	156156434:156156434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.160A>T
AA Mutation	p.Ser54Cys(p.S54C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000355014
Start	156160973:156160973(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.754A>G
AA Mutation	p.Ser252Gly(p.S252G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000355014
Start	156161009:156161009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.790C>T
AA Mutation	p.Arg264Trp(p.R264W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000355014
Start	156175648:156175648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780625142
CDS Mutation	c.1685C>T
AA Mutation	p.Pro562Leu(p.P562L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000355014
Start	156174918:156174918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1412A>G
AA Mutation	p.Asn471Ser(p.N471S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000355014
Start	156172833:156172833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1142T>C
AA Mutation	p.Val381Ala(p.V381A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000355014
Start	156163047:156163047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750520474
CDS Mutation	c.1087C>T
AA Mutation	p.Arg363Cys(p.R363C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000355014
Start	156172982:156172982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1291C>A
AA Mutation	p.His431Asn(p.H431N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000355014
Start	156161368:156161368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.833T>G
AA Mutation	p.Leu278Arg(p.L278R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000355014
Start	156172876:156172876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1185T>A
AA Mutation	p.His395Gln(p.H395Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355014
Start	156172906:156172906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs151260330
CDS Mutation	c.1215G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SEMA4A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000355014
Start	156176684:156176684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747644135
CDS Mutation	c.1973G>A
AA Mutation	p.Arg658Gln(p.R658Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000355014
Start	156163073:156163073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1113G>T
AA Mutation	p.Glu371Asp(p.E371D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript