Colon Cancer: Gene >> SECISBP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375807
Start	89334681:89334681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1040C>T
AA Mutation	p.Ser347Leu(p.S347L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000375807
Start	89350697:89350697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1958T>C
AA Mutation	p.Val653Ala(p.V653A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000375807
Start	89328731:89328731(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.646T>G
AA Mutation	p.Phe216Val(p.F216V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000375807
Start	89346941:89346941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1495A>C
AA Mutation	p.Ser499Arg(p.S499R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375807
Start	89341436:89341436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1392C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375807
Start	89319771:89319771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.156G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375807
Start	89357532:89357532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2235T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375807
Start	89325923:89325923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771723645
CDS Mutation	c.459G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000375807
Start	89350630:89350630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1893-2A>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> SECISBP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375807
Start	89350675:89350675(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1936A>G
AA Mutation	p.Thr646Ala(p.T646A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript