Colon Cancer: Gene >> UNC5A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000329542
Start	176870432:176870432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.784C>T
AA Mutation	p.Arg262Trp(p.R262W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000329542
Start	176877683:176877683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1615T>G
AA Mutation	p.Ser539Ala(p.S539A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000329542
Start	176877976:176877976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1718A>G
AA Mutation	p.Glu573Gly(p.E573G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000329542
Start	176868165:176868165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.328A>G
AA Mutation	p.Arg110Gly(p.R110G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000329542
Start	176870513:176870513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.865A>G
AA Mutation	p.Thr289Ala(p.T289A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000329542
Start	176878057:176878057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1799C>T
AA Mutation	p.Pro600Leu(p.P600L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000329542
Start	176879403:176879403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2278C>T
AA Mutation	p.Arg760Trp(p.R760W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000329542
Start	176870417:176870417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.769G>T
AA Mutation	p.Asp257Tyr(p.D257Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000329542
Start	176870418:176870418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.770A>C
AA Mutation	p.Asp257Ala(p.D257A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329542
Start	176877685:176877685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371948820
CDS Mutation	c.1617G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329542
Start	176862754:176862754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.201C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000329542
Start	176874391:176874391(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1207delC
AA Mutation	p.Leu403TrpfsTer40(p.L403Wfs*40)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000329542
Start	176877208:176877208(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1400delC
AA Mutation	p.Pro467GlnfsTer22(p.P467Qfs*22)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000329542
Start	176878270:176878270(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1901delG
AA Mutation	p.Gly634AspfsTer3(p.G634Dfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000329542
Start	176870474:176870474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.826G>T
AA Mutation	p.Glu276Ter(p.E276*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> UNC5A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000329542
Start	176862775:176862775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.222C>G
AA Mutation	p.Phe74Leu(p.F74L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000329542
Start	176868877:176868877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.634C>T
AA Mutation	p.Arg212Cys(p.R212C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329542
Start	176878100:176878100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1842C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000329542
Start	176878270:176878270(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1901delG
AA Mutation	p.Gly634AspfsTer3(p.G634Dfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript