Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> FN3K

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000300784
Start	82748880:82748880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374429960
CDS Mutation	c.494C>T
AA Mutation	p.Pro165Leu(p.P165L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000300784
Start	82750459:82750459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.634G>A
AA Mutation	p.Ala212Thr(p.A212T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000300784
Start	82750429:82750429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.604G>C
AA Mutation	p.Asp202His(p.D202H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300784
Start	82750503:82750503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.678C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000300784
Start	82750582:82750582(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs776430853
CDS Mutation	c.762delG
AA Mutation	p.Phe255SerfsTer32(p.F255Sfs*32)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000300784
Start	82735756:82735757(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.123dupA
AA Mutation	p.Val42SerfsTer12(p.V42Sfs*12)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> FN3K

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000300784
Start	82750529:82750529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.704C>T
AA Mutation	p.Pro235Leu(p.P235L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000300784
Start	82738579:82738579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.232G>A
AA Mutation	p.Asp78Asn(p.D78N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000300784
Start	82750645:82750645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.820G>A
AA Mutation	p.Asp274Asn(p.D274N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript