Mutation

Primary Site >> Stomach Cancer

Gene >> PRPF3

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000324862
Start	150333095:150333095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.624A>C
AA Mutation	p.Glu208Asp(p.E208D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000324862
Start	150328451:150328451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.408G>T
AA Mutation	p.Met136Ile(p.M136I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000324862
Start	150333181:150333181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.710C>A
AA Mutation	p.Ala237Asp(p.A237D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000324862
Start	150335141:150335141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.935A>G
AA Mutation	p.Asp312Gly(p.D312G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000324862
Start	150328386:150328386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201882091
CDS Mutation	c.343C>T
AA Mutation	p.Arg115Cys(p.R115C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000324862
Start	150333106:150333106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782318341
CDS Mutation	c.635G>A
AA Mutation	p.Arg212Gln(p.R212Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000324862
Start	150346068:150346068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1691C>T
AA Mutation	p.Ala564Val(p.A564V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000324862
Start	150332738:150332738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.478C>A
AA Mutation	p.Leu160Met(p.L160M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324862
Start	150344488:150344488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1581C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000324862
Start	150332728:150332729(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.474dupA
AA Mutation	p.Gln159ThrfsTer6(p.Q159Tfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript