Mutation

Primary Site >> Stomach Cancer

Gene >> PRKD1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000331968
Start	29599672:29599672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2051A>C
AA Mutation	p.Lys684Thr(p.K684T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000331968
Start	29638745:29638745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.856T>C
AA Mutation	p.Tyr286His(p.Y286H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000331968
Start	29666178:29666178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373748041
CDS Mutation	c.434G>A
AA Mutation	p.Arg145His(p.R145H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000331968
Start	29630859:29630859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1555G>A
AA Mutation	p.Val519Ile(p.V519I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000331968
Start	29597547:29597547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2378T>C
AA Mutation	p.Ile793Thr(p.I793T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000331968
Start	29666203:29666203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780784905
CDS Mutation	c.409G>A
AA Mutation	p.Ala137Thr(p.A137T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000331968
Start	29599070:29599070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2123A>G
AA Mutation	p.Lys708Arg(p.K708R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000331968
Start	29631001:29631001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1413T>G
AA Mutation	p.Ile471Met(p.I471M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000331968
Start	29638507:29638507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.967G>A
AA Mutation	p.Glu323Lys(p.E323K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000331968
Start	29597491:29597491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2434G>T
AA Mutation	p.Ala812Ser(p.A812S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000331968
Start	29578354:29578354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2441A>T
AA Mutation	p.Asp814Val(p.D814V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000331968
Start	29725672:29725672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.267C>A
AA Mutation	p.Phe89Leu(p.F89L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000331968
Start	29631005:29631005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1409A>G
AA Mutation	p.Glu470Gly(p.E470G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000331968
Start	29599657:29599657(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2066A>G
AA Mutation	p.Gln689Arg(p.Q689R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000331968
Start	29577315:29577315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2662A>C
AA Mutation	p.Ser888Arg(p.S888R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000331968
Start	29632904:29632904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780895625
CDS Mutation	c.1357C>T
AA Mutation	p.Leu453Phe(p.L453F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000331968
Start	29599058:29599058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2135T>G
AA Mutation	p.Val712Gly(p.V712G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000331968
Start	29666086:29666086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.526A>C
AA Mutation	p.Lys176Gln(p.K176Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000331968
Start	29634527:29634527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1205A>C
AA Mutation	p.Asn402Thr(p.N402T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000331968
Start	29634539:29634539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1193C>T
AA Mutation	p.Pro398Leu(p.P398L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000331968
Start	29666104:29666104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.508C>G
AA Mutation	p.Leu170Val(p.L170V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331968
Start	29599039:29599039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2154T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331968
Start	29626521:29626521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1761A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331968
Start	29599056:29599056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2137T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331968
Start	29597684:29597684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147092748
CDS Mutation	c.2241C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000331968
Start	29634534:29634534(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1198delA
AA Mutation	p.Thr400GlnfsTer8(p.T400Qfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	27
Mutation Consequence	stop_gained
Transcription ID	ENST00000331968
Start	29624223:29624223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1834A>T
AA Mutation	p.Lys612Ter(p.K612*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000331968
Start	29578273:29578273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2520+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript