Mutation

Primary Site >> Stomach Cancer

Gene >> TET1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373644
Start	68690912:68690912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146039331
CDS Mutation	c.5509G>A
AA Mutation	p.Ala1837Thr(p.A1837T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373644
Start	68572580:68572580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761821309
CDS Mutation	c.242G>A
AA Mutation	p.Arg81His(p.R81H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373644
Start	68691207:68691207(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs540373976
CDS Mutation	c.5804C>T
AA Mutation	p.Thr1935Met(p.T1935M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000373644
Start	68686690:68686690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5387C>T
AA Mutation	p.Ser1796Leu(p.S1796L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000373644
Start	68691516:68691516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6113G>A
AA Mutation	p.Arg2038His(p.R2038H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000373644
Start	68644747:68644747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2018A>T
AA Mutation	p.Asp673Val(p.D673V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000373644
Start	68690981:68690981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5578G>C
AA Mutation	p.Ala1860Pro(p.A1860P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000373644
Start	68691201:68691201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765929366
CDS Mutation	c.5798C>T
AA Mutation	p.Pro1933Leu(p.P1933L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000373644
Start	68652520:68652520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4387G>A
AA Mutation	p.Ala1463Thr(p.A1463T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000373644
Start	68646262:68646262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3533A>C
AA Mutation	p.Lys1178Thr(p.K1178T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000373644
Start	68574087:68574087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1749G>T
AA Mutation	p.Leu583Phe(p.L583F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000373644
Start	68646595:68646595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs575341146
CDS Mutation	c.3866C>T
AA Mutation	p.Thr1289Met(p.T1289M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000373644
Start	68686384:68686384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5081G>A
AA Mutation	p.Arg1694His(p.R1694H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373644
Start	68686511:68686511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5208C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373644
Start	68691436:68691436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374115480
CDS Mutation	c.6033C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373644
Start	68667230:68667230(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748841009
CDS Mutation	c.4647C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373644
Start	68690878:68690878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5475A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373644
Start	68573976:68573976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1638C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373644
Start	68691454:68691454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766318386
CDS Mutation	c.6051G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373644
Start	68572812:68572812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.474T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373644
Start	68573655:68573655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1317A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373644
Start	68645849:68645849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3120A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373644
Start	68572396:68572396(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.65delA
AA Mutation	p.Lys22ArgfsTer23(p.K22Rfs*23)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373644
Start	68572516:68572516(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.184delA
AA Mutation	p.Thr62GlnfsTer13(p.T62Qfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373644
Start	68691557:68691557(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.6158delA
AA Mutation	p.Asn2053ThrfsTer2(p.N2053Tfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	26
Mutation Consequence	stop_gained
Transcription ID	ENST00000373644
Start	68686413:68686413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5110C>T
AA Mutation	p.Gln1704Ter(p.Q1704*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373644
Start	68572918:68572919(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.583dupA
AA Mutation	p.Arg195LysfsTer3(p.R195Kfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373644
Start	68572515:68572516(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.184dupA
AA Mutation	p.Thr62AsnfsTer4(p.T62Nfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373644
Start	68686526:68686527(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.5230dupA
AA Mutation	p.Arg1744LysfsTer26(p.R1744Kfs*26)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373644
Start	68691132:68691133(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.5733dupC
AA Mutation	p.Thr1912HisfsTer12(p.T1912Hfs*12)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript