Mutation

Primary Site >> Stomach Cancer

Gene >> TET3

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000409262
Start	74089970:74089970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2962A>G
AA Mutation	p.Met988Val(p.M988V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000409262
Start	74047472:74047472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs539053042
CDS Mutation	c.1555G>A
AA Mutation	p.Asp519Asn(p.D519N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000409262
Start	74089997:74089997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2989C>T
AA Mutation	p.Arg997Trp(p.R997W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000409262
Start	74100833:74100833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4045G>A
AA Mutation	p.Ala1349Thr(p.A1349T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000409262
Start	74090027:74090027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754843346
CDS Mutation	c.3019G>A
AA Mutation	p.Ala1007Thr(p.A1007T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000409262
Start	74101955:74101955(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774264827
CDS Mutation	c.5167C>T
AA Mutation	p.Arg1723Trp(p.R1723W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000409262
Start	74048025:74048025(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2108C>T
AA Mutation	p.Ala703Val(p.A703V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000409262
Start	74046483:74046483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.566C>T
AA Mutation	p.Ala189Val(p.A189V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000409262
Start	74047002:74047002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1085C>G
AA Mutation	p.Ala362Gly(p.A362G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000409262
Start	74099433:74099433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3425T>C
AA Mutation	p.Leu1142Pro(p.L1142P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000409262
Start	74046894:74046894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.977C>T
AA Mutation	p.Ser326Leu(p.S326L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000409262
Start	74101815:74101815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5027C>T
AA Mutation	p.Thr1676Met(p.T1676M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000409262
Start	74101058:74101058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773119673
CDS Mutation	c.4270G>A
AA Mutation	p.Glu1424Lys(p.E1424K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000409262
Start	74046633:74046633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750013561
CDS Mutation	c.716C>T
AA Mutation	p.Pro239Leu(p.P239L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409262
Start	74101741:74101741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs570795230
CDS Mutation	c.4953C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409262
Start	74046523:74046523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.606C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409262
Start	74100784:74100784(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752490503
CDS Mutation	c.3996C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409262
Start	74100625:74100625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376482452
CDS Mutation	c.3837C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409262
Start	74089906:74089906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2898C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000409262
Start	74047949:74047949(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2036delC
AA Mutation	p.Pro679LeufsTer5(p.P679Lfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000409262
Start	74047047:74047047(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1135delC
AA Mutation	p.Gln379ArgfsTer162(p.Q379Rfs*162)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000409262
Start	74046963:74046963(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1052delA
AA Mutation	p.Asn351ThrfsTer190(p.N351Tfs*190)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000409262
Start	74102025:74102025(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.5243delG
AA Mutation	p.Gly1748AlafsTer106(p.G1748Afs*106)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000409262
Start	74048094:74048095(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2183dupC
AA Mutation	p.Ser729PhefsTer18(p.S729Ffs*18)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	25
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000409262
Start	74080496:74080496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2586-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript