Mutation

Primary Site >> Stomach Cancer

Gene >> FOXP4

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000307972
Start	41591261:41591261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1475A>G
AA Mutation	p.Glu492Gly(p.E492G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000307972
Start	41589822:41589822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140387832
CDS Mutation	c.1117C>T
AA Mutation	p.Arg373Trp(p.R373W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
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

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000307972
Start	41597857:41597857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1802T>A
AA Mutation	p.Leu601Gln(p.L601Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000307972
Start	41594879:41594879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1546C>T
AA Mutation	p.Arg516Cys(p.R516C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000307972
Start	41590304:41590304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1391C>A
AA Mutation	p.Ala464Asp(p.A464D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000307972
Start	41590081:41590081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1268G>A
AA Mutation	p.Arg423Gln(p.R423Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307972
Start	41594875:41594875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779810959
CDS Mutation	c.1542C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307972
Start	41565856:41565856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149894394
CDS Mutation	c.96C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307972
Start	41585436:41585436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.429G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	11
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

ID	12
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

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307972
Start	41590043:41590043(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1235delC
AA Mutation	p.Pro412ArgfsTer77(p.P412Rfs*77)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript