Mutation

Primary Site >> Stomach Cancer

Gene >> PCDH20

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000409186
Start	61413229:61413229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.870C>G
AA Mutation	p.Ile290Met(p.I290M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000409186
Start	61411304:61411304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2795T>G
AA Mutation	p.Leu932Arg(p.L932R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000409186
Start	61411485:61411485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2614A>T
AA Mutation	p.Ile872Phe(p.I872F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000409186
Start	61413296:61413296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.803G>A
AA Mutation	p.Arg268His(p.R268H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000409186
Start	61413840:61413840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.259G>A
AA Mutation	p.Glu87Lys(p.E87K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000409186
Start	61412349:61412349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1750T>G
AA Mutation	p.Leu584Val(p.L584V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000409186
Start	61411763:61411763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2336T>C
AA Mutation	p.Val779Ala(p.V779A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000409186
Start	61412778:61412778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1321C>A
AA Mutation	p.Leu441Met(p.L441M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000409186
Start	61413297:61413297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150237018
CDS Mutation	c.802C>T
AA Mutation	p.Arg268Cys(p.R268C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000409186
Start	61412975:61412975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1124A>G
AA Mutation	p.Glu375Gly(p.E375G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000409186
Start	61411527:61411527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2572A>G
AA Mutation	p.Arg858Gly(p.R858G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000409186
Start	61412097:61412097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2002G>C
AA Mutation	p.Ala668Pro(p.A668P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000409186
Start	61411590:61411590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2509G>T
AA Mutation	p.Val837Phe(p.V837F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000409186
Start	61411889:61411889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2210A>G
AA Mutation	p.Asp737Gly(p.D737G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000409186
Start	61411782:61411782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2317G>A
AA Mutation	p.Asp773Asn(p.D773N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000409186
Start	61413753:61413753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750532210
CDS Mutation	c.346C>T
AA Mutation	p.Pro116Ser(p.P116S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000409186
Start	61413058:61413058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1041A>C
AA Mutation	p.Lys347Asn(p.K347N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000409186
Start	61411308:61411308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2791C>T
AA Mutation	p.Pro931Ser(p.P931S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000409186
Start	61412096:61412096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2003C>A
AA Mutation	p.Ala668Asp(p.A668D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000409186
Start	61412195:61412195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1904A>G
AA Mutation	p.Asn635Ser(p.N635S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409186
Start	61413745:61413745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.354C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409186
Start	61413739:61413739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.360C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409186
Start	61412140:61412140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1959A>C
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409186
Start	61412053:61412053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2046T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409186
Start	61413013:61413013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1086A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409186
Start	61413709:61413709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.390C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409186
Start	61413922:61413922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.177C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000409186
Start	61413752:61413752(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.347delC
AA Mutation	p.Pro116LeufsTer11(p.P116Lfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000409186
Start	61413289:61413289(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.810delC
AA Mutation	p.Tyr271ThrfsTer2(p.Y271Tfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	30
Mutation Consequence	stop_gained
Transcription ID	ENST00000409186
Start	61412292:61412292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1807G>T
AA Mutation	p.Glu603Ter(p.E603*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	31
Mutation Consequence	stop_gained
Transcription ID	ENST00000409186
Start	61411476:61411476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2623G>T
AA Mutation	p.Glu875Ter(p.E875*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	32
Mutation Consequence	stop_gained
Transcription ID	ENST00000409186
Start	61411527:61411527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2572A>T
AA Mutation	p.Arg858Ter(p.R858*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	33
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000409186
Start	61412437:61412438(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1661dupT
AA Mutation	p.Leu554PhefsTer3(p.L554Ffs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript