Mutation

Primary Site >> Stomach Cancer

Gene >> PPFIA1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000253925
Start	70354374:70354374(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2237C>T
AA Mutation	p.Pro746Leu(p.P746L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000253925
Start	70375043:70375043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747502376
CDS Mutation	c.3265G>A
AA Mutation	p.Asp1089Asn(p.D1089N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000253925
Start	70356223:70356223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2551C>G
AA Mutation	p.Gln851Glu(p.Q851E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000253925
Start	70375040:70375040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3262T>G
AA Mutation	p.Phe1088Val(p.F1088V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000253925
Start	70372375:70372375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3026T>G
AA Mutation	p.Val1009Gly(p.V1009G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000253925
Start	70272318:70272318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750251702
CDS Mutation	c.146G>A
AA Mutation	p.Arg49His(p.R49H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000253925
Start	70354389:70354389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2252T>C
AA Mutation	p.Leu751Ser(p.L751S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253925
Start	70343836:70343836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745358718
CDS Mutation	c.1875G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253925
Start	70378140:70378140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3495G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000253925
Start	70337394:70337394(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1463delA
AA Mutation	p.Lys488SerfsTer3(p.K488Sfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000253925
Start	70356248:70356248(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2582delA
AA Mutation	p.Lys861SerfsTer27(p.K861Sfs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript