Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> SKAP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000345317
Start	26854801:26854801(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.157A>C
AA Mutation	p.Lys53Gln(p.K53Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000345317
Start	26725454:26725454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.770A>T
AA Mutation	p.Asp257Val(p.D257V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000345317
Start	26854798:26854798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.160G>T
AA Mutation	p.Asp54Tyr(p.D54Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SKAP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000345317
Start	26738841:26738841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.423G>T
AA Mutation	p.Trp141Cys(p.W141C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000345317
Start	26854852:26854852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.106A>C
AA Mutation	p.Asn36His(p.N36H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript