Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> NCF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367535
Start	183565758:183565758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778521448
CDS Mutation	c.946G>A
AA Mutation	p.Asp316Asn(p.D316N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367535
Start	183567215:183567215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.844T>C
AA Mutation	p.Phe282Leu(p.F282L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367535
Start	183556156:183556156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369006606
CDS Mutation	c.1543G>A
AA Mutation	p.Ala515Thr(p.A515T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367535
Start	183577671:183577671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.294G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367535
Start	183586956:183586956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750782115
CDS Mutation	c.196C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367535
Start	183556182:183556182(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1517delT
AA Mutation	p.Phe506SerfsTer30(p.F506Sfs*30)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000367535
Start	183586923:183586923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752901695
CDS Mutation	c.229C>T
AA Mutation	p.Arg77Ter(p.R77*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> NCF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367535
Start	183563491:183563491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1121A>T
AA Mutation	p.Gln374Leu(p.Q374L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367535
Start	183560128:183560128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1436A>T
AA Mutation	p.Gln479Leu(p.Q479L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367535
Start	183564011:183564011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1020G>A
Mutation Classification	Silent
Feature Type	Transcript