Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> FABP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000274024
Start	119319628:119319628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.256G>C
AA Mutation	p.Glu86Gln(p.E86Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000274024
Start	119319598:119319598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753335773
CDS Mutation	c.286C>T
AA Mutation	p.Arg96Trp(p.R96W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274024
Start	119320784:119320784(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.126A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274024
Start	119320754:119320754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.156A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274024
Start	119319599:119319599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.285A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000274024
Start	119320780:119320780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.130G>T
AA Mutation	p.Glu44Ter(p.E44*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000274024
Start	119322038:119322039(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.64dupA
AA Mutation	p.Met22AsnfsTer4(p.M22Nfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> FABP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000274024
Start	119319580:119319580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375920710
CDS Mutation	c.304G>A
AA Mutation	p.Glu102Lys(p.E102K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274024
Start	119320829:119320829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.81G>A
Mutation Classification	Silent
Feature Type	Transcript