Mutation

Primary Site >> Stomach Cancer

Gene >> PIWIL2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356766
Start	22289894:22289894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1034A>G
AA Mutation	p.Asp345Gly(p.D345G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356766
Start	22281479:22281479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.389A>G
AA Mutation	p.Asp130Gly(p.D130G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356766
Start	22318260:22318260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2388A>T
AA Mutation	p.Leu796Phe(p.L796F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000356766
Start	22281124:22281124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.203C>A
AA Mutation	p.Ser68Tyr(p.S68Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000356766
Start	22279568:22279568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.182G>A
AA Mutation	p.Arg61Lys(p.R61K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000356766
Start	22306016:22306016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1545G>T
AA Mutation	p.Lys515Asn(p.K515N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000356766
Start	22353094:22353094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2539A>G
AA Mutation	p.Met847Val(p.M847V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000356766
Start	22355411:22355411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2828C>A
AA Mutation	p.Pro943His(p.P943H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356766
Start	22316304:22316304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs553102129
CDS Mutation	c.2268C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356766
Start	22315118:22315118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2181T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356766
Start	22283139:22283139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753622262
CDS Mutation	c.531G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356766
Start	22283149:22283149(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.545delC
AA Mutation	p.Pro182ArgfsTer23(p.P182Rfs*23)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356766
Start	22318260:22318260(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2393delA
AA Mutation	p.Lys798SerfsTer5(p.K798Sfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356766
Start	22309999:22309999(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1730delA
AA Mutation	p.Asn577IlefsTer10(p.N577Ifs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	15
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000356766
Start	22353213:22353213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2657+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript