Colon Cancer: Gene >> SEMA3B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000616701
Start	50273580:50273580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.856T>C
AA Mutation	p.Phe286Leu(p.F286L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000616701
Start	50275720:50275720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1721C>T
AA Mutation	p.Ala574Val(p.A574V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000616701
Start	50275435:50275435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1625C>T
AA Mutation	p.Thr542Met(p.T542M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000616701
Start	50273770:50273770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.934C>A
AA Mutation	p.Leu312Met(p.L312M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000616701
Start	50274032:50274032(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1112G>A
AA Mutation	p.Arg371His(p.R371H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000616701
Start	50274871:50274871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1386G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000616701
Start	50274925:50274925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1440C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000616701
Start	50276505:50276505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2049G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000616701
Start	50275725:50275725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1726C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000616701
Start	50275779:50275779(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1783delC
AA Mutation	p.Arg595AlafsTer16(p.R595Afs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000616701
Start	50274471:50274471(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1251delG
AA Mutation	p.Arg418AlafsTer41(p.R418Afs*41)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SEMA3B

No Mutation Annotation!