Mutation

Primary Site >> Stomach Cancer

Gene >> TFAP4

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000204517
Start	4261901:4261901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.403G>A
AA Mutation	p.Glu135Lys(p.E135K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000204517
Start	4262645:4262645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.146G>A
AA Mutation	p.Arg49Gln(p.R49Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000204517
Start	4258230:4258230(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.842G>A
AA Mutation	p.Gly281Asp(p.G281D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000204517
Start	4261804:4261804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.500C>T
AA Mutation	p.Ser167Leu(p.S167L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000204517
Start	4261885:4261885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.419C>T
AA Mutation	p.Pro140Leu(p.P140L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000204517
Start	4261898:4261898(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.406G>A
AA Mutation	p.Gly136Ser(p.G136S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000204517
Start	4262643:4262643(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.148C>T
AA Mutation	p.Arg50Trp(p.R50W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000204517
Start	4262612:4262612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.179G>A
AA Mutation	p.Arg60His(p.R60H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000204517
Start	4262651:4262651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.140G>A
AA Mutation	p.Arg47Gln(p.R47Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000204517
Start	4262554:4262554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.237C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000204517
Start	4262635:4262635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777971498
CDS Mutation	c.156C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000204517
Start	4262623:4262623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.168C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000204517
Start	4258072:4258072(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1000delG
AA Mutation	p.Asp334ThrfsTer33(p.D334Tfs*33)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000204517
Start	4258192:4258192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.880C>T
AA Mutation	p.Arg294Ter(p.R294*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript