Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> RASSF8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000282884
Start	26065069:26065069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.675C>A
AA Mutation	p.Phe225Leu(p.F225L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000282884
Start	26064829:26064829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.435A>C
AA Mutation	p.Lys145Asn(p.K145N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000282884
Start	26065017:26065017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs117015558
CDS Mutation	c.623G>A
AA Mutation	p.Arg208His(p.R208H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000282884
Start	26064971:26064971(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.580delT
AA Mutation	p.Trp194GlyfsTer16(p.W194Gfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> RASSF8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000282884
Start	26065038:26065038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.644G>T
AA Mutation	p.Arg215Ile(p.R215I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282884
Start	26065015:26065015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.621C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282884
Start	26055352:26055352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.9T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282884
Start	26065279:26065279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.885C>T
Mutation Classification	Silent
Feature Type	Transcript