Mutation

Primary Site >> Stomach Cancer

Gene >> TJP1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000346128
Start	29718362:29718362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3780G>C
AA Mutation	p.Lys1260Asn(p.K1260N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000346128
Start	29718363:29718363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3779A>C
AA Mutation	p.Lys1260Thr(p.K1260T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000346128
Start	29766446:29766446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202151545
CDS Mutation	c.409C>T
AA Mutation	p.His137Tyr(p.H137Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000346128
Start	29726939:29726939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774071639
CDS Mutation	c.2153A>G
AA Mutation	p.Tyr718Cys(p.Y718C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000346128
Start	29718303:29718303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3839A>C
AA Mutation	p.Glu1280Ala(p.E1280A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000346128
Start	29719050:29719050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3092C>A
AA Mutation	p.Pro1031Gln(p.P1031Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000346128
Start	29718502:29718502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3640T>G
AA Mutation	p.Phe1214Val(p.F1214V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000346128
Start	29716746:29716746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762084848
CDS Mutation	c.4067G>A
AA Mutation	p.Arg1356Gln(p.R1356Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000346128
Start	29742671:29742671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1121G>T
AA Mutation	p.Arg374Ile(p.R374I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000346128
Start	29716687:29716687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4126G>A
AA Mutation	p.Ala1376Thr(p.A1376T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000346128
Start	29718567:29718567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3575T>C
AA Mutation	p.Phe1192Ser(p.F1192S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000346128
Start	29718511:29718511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3631G>T
AA Mutation	p.Ala1211Ser(p.A1211S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000346128
Start	29726957:29726957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2135C>A
AA Mutation	p.Ala712Glu(p.A712E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000346128
Start	29800647:29800647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.83G>T
AA Mutation	p.Arg28Met(p.R28M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000346128
Start	29726437:29726437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2354C>T
AA Mutation	p.Ala785Val(p.A785V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000346128
Start	29737323:29737323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1348G>A
AA Mutation	p.Val450Ile(p.V450I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000346128
Start	29705696:29705696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4900G>A
AA Mutation	p.Ala1634Thr(p.A1634T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000346128
Start	29726930:29726930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2162G>T
AA Mutation	p.Trp721Leu(p.W721L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000346128
Start	29773317:29773317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.125G>A
AA Mutation	p.Arg42Gln(p.R42Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000346128
Start	29718516:29718516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3626C>T
AA Mutation	p.Ser1209Phe(p.S1209F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000346128
Start	29710831:29710831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4372G>T
AA Mutation	p.Gly1458Cys(p.G1458C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000346128
Start	29705590:29705590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201192620
CDS Mutation	c.5006A>G
AA Mutation	p.Gln1669Arg(p.Q1669R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346128
Start	29701613:29701613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5229C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346128
Start	29773265:29773265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774428839
CDS Mutation	c.177G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346128
Start	29737330:29737330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1341A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346128
Start	29718638:29718638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3504T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346128
Start	29719115:29719115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs45562135
CDS Mutation	c.3027C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346128
Start	29761162:29761162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770559228
CDS Mutation	c.987G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000346128
Start	29705662:29705662(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4934delG
AA Mutation	p.Gly1645AlafsTer3(p.G1645Afs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000346128
Start	29732500:29732500(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1950delT
AA Mutation	p.Phe650LeufsTer4(p.F650Lfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	31
Mutation Consequence	stop_gained
Transcription ID	ENST00000346128
Start	29708941:29708941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775677800
CDS Mutation	c.4468C>T
AA Mutation	p.Arg1490Ter(p.R1490*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	32
Mutation Consequence	stop_gained
Transcription ID	ENST00000346128
Start	29718907:29718907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3235C>T
AA Mutation	p.Arg1079Ter(p.R1079*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	33
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000346128
Start	29773300:29773301(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.141dupT
AA Mutation	p.Gln48SerfsTer19(p.Q48Sfs*19)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	34
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000346128
Start	29732529:29732529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1922-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript