Colon Cancer: Gene >> SEMA3C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265361
Start	80810683:80810683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.466G>A
AA Mutation	p.Asp156Asn(p.D156N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265361
Start	80828721:80828721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.128A>C
AA Mutation	p.Glu43Ala(p.E43A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265361
Start	80744964:80744964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2186A>G
AA Mutation	p.Tyr729Cys(p.Y729C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265361
Start	80761623:80761623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1478C>A
AA Mutation	p.Ser493Tyr(p.S493Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265361
Start	80818375:80818375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765250284
CDS Mutation	c.371G>A
AA Mutation	p.Arg124His(p.R124H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265361
Start	80800775:80800775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.968G>A
AA Mutation	p.Gly323Asp(p.G323D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000265361
Start	80745192:80745192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1958C>T
AA Mutation	p.Thr653Ile(p.T653I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000265361
Start	80789312:80789312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367759300
CDS Mutation	c.1348G>A
AA Mutation	p.Gly450Arg(p.G450R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000265361
Start	80789395:80789395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780344553
CDS Mutation	c.1265G>A
AA Mutation	p.Arg422His(p.R422H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000265361
Start	80758332:80758332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775561770
CDS Mutation	c.1642C>T
AA Mutation	p.Arg548Trp(p.R548W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000265361
Start	80789345:80789345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1315G>A
AA Mutation	p.Ala439Thr(p.A439T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000265361
Start	80805698:80805698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774335715
CDS Mutation	c.599G>A
AA Mutation	p.Arg200Gln(p.R200Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000265361
Start	80804224:80804224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.683T>C
AA Mutation	p.Val228Ala(p.V228A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000265361
Start	80758372:80758372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1602G>T
AA Mutation	p.Trp534Cys(p.W534C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000265361
Start	80761626:80761626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1475C>T
AA Mutation	p.Ser492Leu(p.S492L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000265361
Start	80789521:80789521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781697636
CDS Mutation	c.1139G>A
AA Mutation	p.Gly380Glu(p.G380E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000265361
Start	80758419:80758419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1555A>G
AA Mutation	p.Thr519Ala(p.T519A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000265361
Start	80751329:80751329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138526129
CDS Mutation	c.1651C>T
AA Mutation	p.Arg551Ter(p.R551*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000265361
Start	80804117:80804117(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.790C>T
AA Mutation	p.Arg264Ter(p.R264*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	stop_gained;frameshift_variant
Transcription ID	ENST00000265361
Start	80805696:80805697(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.600_601insTAGAATTAAATAAGTT
AA Mutation	p.Ser201Ter(p.S201*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000265361
Start	80804249:80804249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.659-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> SEMA3C

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000265361
Start	80765241:80765241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147463830
CDS Mutation	c.1357C>T
AA Mutation	p.Arg453Trp(p.R453W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265361
Start	80916778:80916778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4G>A
AA Mutation	p.Ala2Thr(p.A2T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265361
Start	80748975:80748975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1765T>G
AA Mutation	p.Phe589Val(p.F589V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript