Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> FOXP4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000307972
Start	41590059:41590059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767113603
CDS Mutation	c.1246G>A
AA Mutation	p.Ala416Thr(p.A416T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000307972
Start	41590324:41590324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1411A>G
AA Mutation	p.Thr471Ala(p.T471A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307972
Start	41598843:41598843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375063628
CDS Mutation	c.1950C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307972
Start	41587423:41587423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375722090
CDS Mutation	c.783G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307972
Start	41587433:41587433(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.798delC
AA Mutation	p.Lys267ArgfsTer100(p.K267Rfs*100)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307972
Start	41587448:41587448(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.814delC
AA Mutation	p.Leu272SerfsTer95(p.L272Sfs*95)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307972
Start	41590042:41590043(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs749833966
CDS Mutation	c.1235dupC
AA Mutation	p.Thr413AspfsTer32(p.T413Dfs*32)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> FOXP4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000307972
Start	41590132:41590132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs576059149
CDS Mutation	c.1319G>A
AA Mutation	p.Arg440Gln(p.R440Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000307972
Start	41565867:41565867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.107G>T
AA Mutation	p.Gly36Val(p.G36V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000307972
Start	41588693:41588693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1027C>T
AA Mutation	p.Arg343Trp(p.R343W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307972
Start	41587447:41587448(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs758240552
CDS Mutation	c.814dupC
AA Mutation	p.Leu272ProfsTer44(p.L272Pfs*44)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript