Mutation

Primary Site >> Stomach Cancer

Gene >> TSHZ2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371497
Start	53254051:53254051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.593A>G
AA Mutation	p.Tyr198Cys(p.Y198C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371497
Start	53254935:53254935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1477G>A
AA Mutation	p.Asp493Asn(p.D493N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371497
Start	53256137:53256137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2679G>A
AA Mutation	p.Met893Ile(p.M893I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000371497
Start	53254902:53254902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200752097
CDS Mutation	c.1444G>A
AA Mutation	p.Glu482Lys(p.E482K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000371497
Start	53254389:53254389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.931A>C
AA Mutation	p.Thr311Pro(p.T311P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000371497
Start	53254105:53254105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145172538
CDS Mutation	c.647G>A
AA Mutation	p.Arg216Gln(p.R216Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000371497
Start	53253744:53253744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.286A>G
AA Mutation	p.Lys96Glu(p.K96E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000371497
Start	53253540:53253540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.82A>C
AA Mutation	p.Lys28Gln(p.K28Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000371497
Start	53255847:53255847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776055494
CDS Mutation	c.2389G>A
AA Mutation	p.Asp797Asn(p.D797N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000371497
Start	53255574:53255574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2116T>A
AA Mutation	p.Leu706Met(p.L706M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000371497
Start	53255361:53255361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61760184
CDS Mutation	c.1903C>T
AA Mutation	p.Arg635Cys(p.R635C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000371497
Start	53254364:53254364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.906A>C
AA Mutation	p.Lys302Asn(p.K302N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000371497
Start	53255423:53255423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1965G>T
AA Mutation	p.Glu655Asp(p.E655D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000371497
Start	53255521:53255521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2063C>A
AA Mutation	p.Ala688Asp(p.A688D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000371497
Start	53255745:53255745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2287C>A
AA Mutation	p.Gln763Lys(p.Q763K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000371497
Start	53254322:53254322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.864A>C
AA Mutation	p.Gln288His(p.Q288H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000371497
Start	53255728:53255728(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2270T>G
AA Mutation	p.Leu757Arg(p.L757R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000371497
Start	53254444:53254444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.986G>T
AA Mutation	p.Arg329Leu(p.R329L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000371497
Start	53256294:53256294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2836G>C
AA Mutation	p.Glu946Gln(p.E946Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000371497
Start	53256103:53256103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2645G>A
AA Mutation	p.Arg882His(p.R882H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000371497
Start	53256490:53256490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3032T>G
AA Mutation	p.Leu1011Arg(p.L1011R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371497
Start	53255498:53255498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770819228
CDS Mutation	c.2040C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371497
Start	53253611:53253611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.153C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371497
Start	53256188:53256188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372585322
CDS Mutation	c.2730G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371497
Start	53255429:53255429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1971G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371497
Start	53255684:53255684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2226G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371497
Start	53256089:53256089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2631G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371497
Start	53254751:53254751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749447914
CDS Mutation	c.1293G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371497
Start	53255375:53255375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1917A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371497
Start	53255351:53255351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749657103
CDS Mutation	c.1893C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371497
Start	53256299:53256299(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2841T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371497
Start	53255053:53255053(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1598delA
AA Mutation	p.Asn533ThrfsTer43(p.N533Tfs*43)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	33
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371497
Start	53254453:53254453(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.999delC
AA Mutation	p.Asp334IlefsTer47(p.D334Ifs*47)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	34
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371497
Start	53255906:53255906(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2454delC
AA Mutation	p.Met819Ter(p.M819*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	35
Mutation Consequence	stop_gained
Transcription ID	ENST00000371497
Start	53254515:53254515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1057C>T
AA Mutation	p.Gln353Ter(p.Q353*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	36
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371497
Start	53255905:53255906(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2454dupC
AA Mutation	p.Met819HisfsTer11(p.M819Hfs*11)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript