Mutation

Primary Site >> Stomach Cancer

Gene >> PARD3

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374789
Start	34269685:34269685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138980029
CDS Mutation	c.3400C>T
AA Mutation	p.Arg1134Trp(p.R1134W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374789
Start	34341645:34341645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2399T>A
AA Mutation	p.Ile800Asn(p.I800N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374789
Start	34284207:34284207(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374258573
CDS Mutation	c.3113C>T
AA Mutation	p.Thr1038Met(p.T1038M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000374789
Start	34384147:34384147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752993561
CDS Mutation	c.998G>A
AA Mutation	p.Arg333Gln(p.R333Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000374789
Start	34374956:34374956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1586C>T
AA Mutation	p.Ser529Leu(p.S529L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000374789
Start	34341771:34341771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2273C>T
AA Mutation	p.Thr758Ile(p.T758I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000374789
Start	34360124:34360124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774764458
CDS Mutation	c.1843G>A
AA Mutation	p.Ala615Thr(p.A615T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000374789
Start	34119634:34119634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752058745
CDS Mutation	c.3656G>A
AA Mutation	p.Arg1219His(p.R1219H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000374789
Start	34111362:34111362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754665239
CDS Mutation	c.3878G>A
AA Mutation	p.Arg1293Gln(p.R1293Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000374789
Start	34331273:34331273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762819451
CDS Mutation	c.2686G>A
AA Mutation	p.Ala896Thr(p.A896T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000374789
Start	34382656:34382656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141769427
CDS Mutation	c.1283C>T
AA Mutation	p.Ser428Leu(p.S428L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000374789
Start	34331137:34331137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2822A>G
AA Mutation	p.Asp941Gly(p.D941G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000374789
Start	34450435:34450435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs192803216
CDS Mutation	c.596A>G
AA Mutation	p.Tyr199Cys(p.Y199C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000374789
Start	34337349:34337349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs562286256
CDS Mutation	c.2495G>A
AA Mutation	p.Arg832His(p.R832H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374789
Start	34119657:34119657(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3633C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374789
Start	34111427:34111427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760990072
CDS Mutation	c.3813A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374789
Start	34269776:34269776(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3309T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374789
Start	34341737:34341737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2307T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374789
Start	34331151:34331151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763973634
CDS Mutation	c.2808C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374789
Start	34399383:34399383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764181890
CDS Mutation	c.837C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374789
Start	34119714:34119714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745473559
CDS Mutation	c.3576C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374789
Start	34470186:34470186(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.481delT
AA Mutation	p.Ser161ProfsTer62(p.S161Pfs*62)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374789
Start	34111199:34111205(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4035_4041delTCAGACT
AA Mutation	p.Gln1346LeufsTer114(p.Q1346Lfs*114)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374789
Start	34382573:34382573(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1366delA
AA Mutation	p.Ile456Ter(p.I456*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	25
Mutation Consequence	stop_gained
Transcription ID	ENST00000374789
Start	34337380:34337380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2464G>T
AA Mutation	p.Gly822Ter(p.G822*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000374789
Start	34378107:34378107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1400-1G>C
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	27
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000374789
Start	34337428:34337428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2418-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	28
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000374789
Start	34470083:34470083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.582+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript