Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> HNRNPF

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000337970
Start	43387548:43387548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.337G>A
AA Mutation	p.Val113Met(p.V113M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000337970
Start	43386996:43386996(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.889C>T
AA Mutation	p.Pro297Ser(p.P297S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000337970
Start	43387357:43387357(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.528A>G
AA Mutation	p.Ile176Met(p.I176M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000337970
Start	43387495:43387495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.390C>A
AA Mutation	p.Phe130Leu(p.F130L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000337970
Start	43386789:43386789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1096G>T
AA Mutation	p.Gly366Trp(p.G366W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000337970
Start	43387590:43387590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.295C>T
AA Mutation	p.His99Tyr(p.H99Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000337970
Start	43387549:43387549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753415568
CDS Mutation	c.336C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000337970
Start	43387612:43387612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.273C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> HNRNPF

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000337970
Start	43387563:43387563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.322G>A
AA Mutation	p.Ala108Thr(p.A108T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000337970
Start	43387548:43387548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.337G>A
AA Mutation	p.Val113Met(p.V113M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000337970
Start	43387417:43387417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763366937
CDS Mutation	c.468C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000337970
Start	43387539:43387539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760246508
CDS Mutation	c.346C>T
AA Mutation	p.Arg116Ter(p.R116*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript