Mutation

Primary Site >> Stomach Cancer

Gene >> CHD3

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000330494
Start	7893838:7893838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749330456
CDS Mutation	c.827G>A
AA Mutation	p.Arg276Gln(p.R276Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000330494
Start	7903335:7903335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3559C>T
AA Mutation	p.Arg1187Cys(p.R1187C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000330494
Start	7910538:7910538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765857922
CDS Mutation	c.5701C>T
AA Mutation	p.Arg1901Cys(p.R1901C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000330494
Start	7895370:7895370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1535T>A
AA Mutation	p.Ile512Asn(p.I512N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000330494
Start	7906929:7906929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4564A>C
AA Mutation	p.Ser1522Arg(p.S1522R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000330494
Start	7890707:7890707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.350G>A
AA Mutation	p.Arg117Gln(p.R117Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000330494
Start	7899901:7899901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2550G>T
AA Mutation	p.Glu850Asp(p.E850D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000330494
Start	7895382:7895382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1547G>A
AA Mutation	p.Arg516Gln(p.R516Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000330494
Start	7907471:7907471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4907G>T
AA Mutation	p.Gly1636Val(p.G1636V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000330494
Start	7905687:7905687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4205G>A
AA Mutation	p.Arg1402Gln(p.R1402Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000330494
Start	7895028:7895028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769962813
CDS Mutation	c.1381G>A
AA Mutation	p.Val461Ile(p.V461I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000330494
Start	7910878:7910878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs561278276
CDS Mutation	c.5786C>T
AA Mutation	p.Pro1929Leu(p.P1929L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000330494
Start	7894241:7894241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771669987
CDS Mutation	c.1051C>T
AA Mutation	p.Arg351Trp(p.R351W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000330494
Start	7910934:7910934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5842G>A
AA Mutation	p.Ala1948Thr(p.A1948T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000330494
Start	7900028:7900028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2677T>C
AA Mutation	p.Ser893Pro(p.S893P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000330494
Start	7905918:7905918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4287G>A
AA Mutation	p.Met1429Ile(p.M1429I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000330494
Start	7902671:7902671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3314G>A
AA Mutation	p.Arg1105His(p.R1105H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000330494
Start	7910478:7910478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5641C>T
AA Mutation	p.Arg1881Cys(p.R1881C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000330494
Start	7908713:7908713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5278T>C
AA Mutation	p.Trp1760Arg(p.W1760R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000330494
Start	7906910:7906910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779331791
CDS Mutation	c.4545G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000330494
Start	7911531:7911531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371864899
CDS Mutation	c.5949C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000330494
Start	7890987:7890987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.432G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000330494
Start	7908012:7908012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs570684756
CDS Mutation	c.5145C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000330494
Start	7891029:7891029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.474G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000330494
Start	7894539:7894539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1200C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000330494
Start	7893509:7893509(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.737delC
AA Mutation	p.Pro246LeufsTer49(p.P246Lfs*49)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000330494
Start	7905911:7905911(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4284delG
AA Mutation	p.Met1429CysfsTer16(p.M1429Cfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000330494
Start	7890730:7890730(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.378delG
AA Mutation	p.Gln127LysfsTer14(p.Q127Kfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000330494
Start	7895447:7895447(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1618delC
AA Mutation	p.Arg540ValfsTer16(p.R540Vfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	30
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000330494
Start	7910973:7910974(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.5881_5881+1insCCGCCACCAACGGCCCTCCAGTGCTT
AA Mutation	p.Val1970ProfsTer10(p.V1970Pfs*10)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript