Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> FMN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000559047
Start	32798819:32798819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4115A>C
AA Mutation	p.Asn1372Thr(p.N1372T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000559047
Start	32798936:32798936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374934202
CDS Mutation	c.3998G>A
AA Mutation	p.Arg1333Gln(p.R1333Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000559047
Start	32776885:32776885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4165A>G
AA Mutation	p.Thr1389Ala(p.T1389A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000559047
Start	32900113:32900113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3520G>A
AA Mutation	p.Val1174Met(p.V1174M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000559047
Start	32798937:32798937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3997C>T
AA Mutation	p.Arg1333Ter(p.R1333*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> FMN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000559047
Start	32901921:32901921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3497G>A
AA Mutation	p.Arg1166Gln(p.R1166Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000559047
Start	32926236:32926236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3164G>A
AA Mutation	p.Arg1055Gln(p.R1055Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000559047
Start	32798813:32798813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4121C>A
AA Mutation	p.Ser1374Tyr(p.S1374Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000559047
Start	32888202:32888202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3805G>T
AA Mutation	p.Asp1269Tyr(p.D1269Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000559047
Start	32969421:32969421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2280G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000559047
Start	32968840:32968840(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2861delC
AA Mutation	p.Pro954HisfsTer29(p.P954Hfs*29)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript