Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> SDCCAG8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000366541
Start	243344267:243344267(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1409A>C
AA Mutation	p.Glu470Ala(p.E470A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000366541
Start	243316811:243316811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs35859404
CDS Mutation	c.986C>T
AA Mutation	p.Thr329Met(p.T329M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000366541
Start	243274585:243274585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.349G>A
AA Mutation	p.Asp117Asn(p.D117N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000366541
Start	243330671:243330671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1200A>C
AA Mutation	p.Glu400Asp(p.E400D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000366541
Start	243293142:243293142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748257473
CDS Mutation	c.598G>A
AA Mutation	p.Glu200Lys(p.E200K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000366541
Start	243293199:243293199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.655G>T
AA Mutation	p.Ala219Ser(p.A219S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000366541
Start	243341054:243341054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1237C>T
AA Mutation	p.Gln413Ter(p.Q413*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SDCCAG8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000366541
Start	243308090:243308090(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.842G>C
AA Mutation	p.Gly281Ala(p.G281A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000366541
Start	243426543:243426543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1970A>G
AA Mutation	p.Glu657Gly(p.E657G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000366541
Start	243316886:243316886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1061A>T
AA Mutation	p.Lys354Ile(p.K354I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000366541
Start	243316888:243316888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1063A>T
AA Mutation	p.Thr355Ser(p.T355S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366541
Start	243286322:243286322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769881390
CDS Mutation	c.471C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366541
Start	243308167:243308167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.919A>C
Mutation Classification	Silent
Feature Type	Transcript