Mutation

Primary Site >> Stomach Cancer

Gene >> ATRX

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373344
Start	77681574:77681574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782743875
CDS Mutation	c.3682C>T
AA Mutation	p.Pro1228Ser(p.P1228S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373344
Start	77682453:77682453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2803G>A
AA Mutation	p.Glu935Lys(p.E935K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373344
Start	77684426:77684426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.830T>C
AA Mutation	p.Val277Ala(p.V277A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000373344
Start	77682909:77682909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2347A>C
AA Mutation	p.Ser783Arg(p.S783R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000373344
Start	77684219:77684219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1037T>C
AA Mutation	p.Leu346Pro(p.L346P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000373344
Start	77633378:77633378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4963G>A
AA Mutation	p.Glu1655Lys(p.E1655K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000373344
Start	77676241:77676241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371187842
CDS Mutation	c.3794A>G
AA Mutation	p.Asn1265Ser(p.N1265S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000373344
Start	77664707:77664707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3881A>G
AA Mutation	p.Asp1294Gly(p.D1294G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000373344
Start	77520912:77520912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7076A>G
AA Mutation	p.Lys2359Arg(p.K2359R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000373344
Start	77682527:77682527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2729A>C
AA Mutation	p.Lys910Thr(p.K910T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000373344
Start	77620464:77620464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5203A>G
AA Mutation	p.Met1735Val(p.M1735V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000373344
Start	77682689:77682689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2567G>A
AA Mutation	p.Ser856Asn(p.S856N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000373344
Start	77663455:77663455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4047C>A
AA Mutation	p.Asp1349Glu(p.D1349E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000373344
Start	77684430:77684430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.826T>G
AA Mutation	p.Leu276Val(p.L276V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000373344
Start	77663408:77663408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4094A>C
AA Mutation	p.Glu1365Ala(p.E1365A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000373344
Start	77684478:77684478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.778A>C
AA Mutation	p.Asn260His(p.N260H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000373344
Start	77558670:77558670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6503A>G
AA Mutation	p.Gln2168Arg(p.Q2168R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000373344
Start	77683017:77683017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2239A>G
AA Mutation	p.Ser747Gly(p.S747G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373344
Start	77599800:77599800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5718T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373344
Start	77508369:77508369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7461C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373344
Start	77688866:77688866(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375794120
CDS Mutation	c.546A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373344
Start	77664684:77664684(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3904delA
AA Mutation	p.Arg1302GlufsTer44(p.R1302Efs*44)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373344
Start	77682089:77682089(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3167delA
AA Mutation	p.Lys1056ArgfsTer62(p.K1056Rfs*62)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373344
Start	77663432:77663432(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4070delA
AA Mutation	p.Lys1357ArgfsTer18(p.K1357Rfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373344
Start	77684134:77684135(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1121dupT
AA Mutation	p.Leu374PhefsTer7(p.L374Ffs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373344
Start	77682277:77682278(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2978dupA
AA Mutation	p.Lys994GlufsTer6(p.K994Efs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373344
Start	77574350:77574351(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.6225dupG
AA Mutation	p.Lys2076GlufsTer7(p.K2076Efs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	28
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000373344
Start	77652112:77652112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4557+2T>G
Mutation Classification	Splice_Site
Feature Type	Transcript