Mutation

Primary Site >> Stomach Cancer

Gene >> PKD2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000237596
Start	88074825:88074825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2536G>A
AA Mutation	p.Val846Met(p.V846M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000237596
Start	88067932:88067932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2393G>A
AA Mutation	p.Arg798His(p.R798H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000237596
Start	88019547:88019547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.685C>A
AA Mutation	p.Leu229Ile(p.L229I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000237596
Start	88074906:88074906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2617G>A
AA Mutation	p.Ala873Thr(p.A873T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000237596
Start	88036225:88036225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.715T>C
AA Mutation	p.Tyr239His(p.Y239H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000237596
Start	88019552:88019552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.690T>A
AA Mutation	p.Phe230Leu(p.F230L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000237596
Start	88074831:88074831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2542C>T
AA Mutation	p.Arg848Trp(p.R848W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000237596
Start	88068038:88068038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs180709531
CDS Mutation	c.2499C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000237596
Start	88074872:88074872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369520452
CDS Mutation	c.2583C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000237596
Start	88065768:88065768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2247C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000237596
Start	88058099:88058099(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2018delT
AA Mutation	p.Leu673Ter(p.L673*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000237596
Start	88061912:88061912(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2030delT
AA Mutation	p.Leu677TrpfsTer11(p.L677Wfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000237596
Start	88065406:88065407(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2159dupA
AA Mutation	p.Asn720LysfsTer5(p.N720Kfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript