Colon Cancer: Gene >> SEMA4C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000305476
Start	96866335:96866335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759619456
CDS Mutation	c.206C>T
AA Mutation	p.Ala69Val(p.A69V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000305476
Start	96861068:96861068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768689685
CDS Mutation	c.2060G>A
AA Mutation	p.Arg687His(p.R687H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000305476
Start	96861084:96861084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2044C>G
AA Mutation	p.Leu682Val(p.L682V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000305476
Start	96860684:96860684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2444G>A
AA Mutation	p.Arg815His(p.R815H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000305476
Start	96861179:96861179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1949C>T
AA Mutation	p.Ser650Leu(p.S650L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000305476
Start	96866417:96866417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.124G>A
AA Mutation	p.Val42Ile(p.V42I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000305476
Start	96864865:96864865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752887211
CDS Mutation	c.802G>A
AA Mutation	p.Ala268Thr(p.A268T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000305476
Start	96861846:96861846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs535051646
CDS Mutation	c.1492G>A
AA Mutation	p.Ala498Thr(p.A498T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000305476
Start	96860966:96860966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs541764126
CDS Mutation	c.2162G>A
AA Mutation	p.Arg721Gln(p.R721Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305476
Start	96861796:96861796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1542C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SEMA4C

No Mutation Annotation!