Colon Cancer: Gene >> SEMA6B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000586582
Start	4558351:4558351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.107T>C
AA Mutation	p.Val36Ala(p.V36A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000586582
Start	4555546:4555546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777813030
CDS Mutation	c.490G>A
AA Mutation	p.Val164Ile(p.V164I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000586582
Start	4544436:4544436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1832C>T
AA Mutation	p.Ala611Val(p.A611V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000586582
Start	4544416:4544416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1852G>A
AA Mutation	p.Val618Met(p.V618M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000586582
Start	4550832:4550832(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373900501
CDS Mutation	c.1088C>T
AA Mutation	p.Thr363Met(p.T363M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000586582
Start	4550268:4550268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769299847
CDS Mutation	c.1126G>A
AA Mutation	p.Gly376Arg(p.G376R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000586582
Start	4558057:4558057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.214C>T
AA Mutation	p.Arg72Trp(p.R72W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000586582
Start	4550886:4550886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1034C>T
AA Mutation	p.Ala345Val(p.A345V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000586582
Start	4557209:4557209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.260G>A
AA Mutation	p.Arg87His(p.R87H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000586582
Start	4550829:4550829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs547783583
CDS Mutation	c.1091C>T
AA Mutation	p.Pro364Leu(p.P364L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000586582
Start	4555481:4555481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.555C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000586582
Start	4550149:4550149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144907430
CDS Mutation	c.1245G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000586582
Start	4552585:4552585(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.826delC
AA Mutation	p.Arg276AlafsTer11(p.R276Afs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SEMA6B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000586582
Start	4554422:4554422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370318420
CDS Mutation	c.737G>A
AA Mutation	p.Arg246Gln(p.R246Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000586582
Start	4556986:4556986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.334G>A
AA Mutation	p.Asp112Asn(p.D112N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000586582
Start	4550904:4550904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1016T>C
AA Mutation	p.Phe339Ser(p.F339S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000586582
Start	4552507:4552507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.904T>G
AA Mutation	p.Phe302Val(p.F302V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript