Mutation

Primary Site >> Stomach Cancer

Gene >> FOXP2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000350908
Start	114662135:114662135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1718G>T
AA Mutation	p.Trp573Leu(p.W573L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000350908
Start	114629992:114629992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.584A>G
AA Mutation	p.Lys195Arg(p.K195R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000350908
Start	114642554:114642554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.920C>A
AA Mutation	p.Ala307Glu(p.A307E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000350908
Start	114664354:114664354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745987986
CDS Mutation	c.1921G>A
AA Mutation	p.Val641Ile(p.V641I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000350908
Start	114659629:114659629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1603A>C
AA Mutation	p.Thr535Pro(p.T535P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000350908
Start	114644708:114644708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1013C>T
AA Mutation	p.Ala338Val(p.A338V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000350908
Start	114534621:114534621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.173T>G
AA Mutation	p.Leu58Arg(p.L58R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000350908
Start	114631694:114631694(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.764C>T
AA Mutation	p.Ser255Leu(p.S255L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000350908
Start	114659666:114659666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1640C>A
AA Mutation	p.Thr547Asn(p.T547N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000350908
Start	114664370:114664370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145154396
CDS Mutation	c.1937A>G
AA Mutation	p.Asn646Ser(p.N646S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000350908
Start	114659635:114659635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1609A>G
AA Mutation	p.Thr537Ala(p.T537A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000350908
Start	114662084:114662084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1667T>G
AA Mutation	p.Leu556Arg(p.L556R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000350908
Start	114664430:114664430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145254341
CDS Mutation	c.1997C>T
AA Mutation	p.Pro666Leu(p.P666L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000350908
Start	114663451:114663451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1771A>C
AA Mutation	p.Ser591Arg(p.S591R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000350908
Start	114629998:114629998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769729974
CDS Mutation	c.590C>T
AA Mutation	p.Ala197Val(p.A197V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350908
Start	114658095:114658095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1296G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350908
Start	114658131:114658131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1332T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350908
Start	114664296:114664296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1863A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350908
Start	114629933:114629933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778496902
CDS Mutation	c.525G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000350908
Start	114658225:114658225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1426C>T
AA Mutation	p.Arg476Ter(p.R476*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000350908
Start	114659670:114659670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1644G>A
AA Mutation	p.Trp548Ter(p.W548*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000350908
Start	114663464:114663465(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1790dupA
AA Mutation	p.Asn597LysfsTer13(p.N597Kfs*13)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript