Mutation

Primary Site >> Stomach Cancer

Gene >> CHD5

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262450
Start	6129051:6129051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3406C>T
AA Mutation	p.Arg1136Cys(p.R1136C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262450
Start	6168163:6168163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761147748
CDS Mutation	c.194G>A
AA Mutation	p.Arg65Gln(p.R65Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262450
Start	6149332:6149332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1075G>A
AA Mutation	p.Asp359Asn(p.D359N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262450
Start	6128910:6128910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3547T>C
AA Mutation	p.Ser1183Pro(p.S1183P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262450
Start	6131687:6131687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3206G>A
AA Mutation	p.Arg1069Gln(p.R1069Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262450
Start	6142514:6142514(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2135G>A
AA Mutation	p.Arg712His(p.R712H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000262450
Start	6144066:6144066(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1892T>C
AA Mutation	p.Ile631Thr(p.I631T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000262450
Start	6128966:6128966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3491G>A
AA Mutation	p.Arg1164His(p.R1164H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000262450
Start	6129045:6129045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3412G>A
AA Mutation	p.Gly1138Ser(p.G1138S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000262450
Start	6142135:6142135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147522329
CDS Mutation	c.2429G>A
AA Mutation	p.Arg810His(p.R810H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000262450
Start	6152511:6152511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.771A>C
AA Mutation	p.Lys257Asn(p.K257N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000262450
Start	6112277:6112277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5003A>T
AA Mutation	p.Asp1668Val(p.D1668V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000262450
Start	6154723:6154723(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.682G>A
AA Mutation	p.Val228Ile(p.V228I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000262450
Start	6109900:6109900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5473C>T
AA Mutation	p.Leu1825Phe(p.L1825F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000262450
Start	6136750:6136750(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2552G>A
AA Mutation	p.Arg851His(p.R851H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000262450
Start	6124013:6124013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201559496
CDS Mutation	c.4634C>T
AA Mutation	p.Ser1545Leu(p.S1545L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000262450
Start	6126613:6126613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4037G>A
AA Mutation	p.Arg1346His(p.R1346H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000262450
Start	6142325:6142325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2239C>A
AA Mutation	p.His747Asn(p.H747N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000262450
Start	6121225:6121225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761874883
CDS Mutation	c.4792G>A
AA Mutation	p.Ala1598Thr(p.A1598T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000262450
Start	6146407:6146407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1607C>T
AA Mutation	p.Thr536Met(p.T536M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000262450
Start	6124582:6124582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761795865
CDS Mutation	c.4474C>T
AA Mutation	p.Arg1492Trp(p.R1492W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000262450
Start	6154767:6154767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767762669
CDS Mutation	c.638T>C
AA Mutation	p.Val213Ala(p.V213A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000262450
Start	6128060:6128060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3889G>A
AA Mutation	p.Glu1297Lys(p.E1297K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000262450
Start	6129005:6129005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3452G>A
AA Mutation	p.Arg1151Gln(p.R1151Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000262450
Start	6144039:6144039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1919C>T
AA Mutation	p.Ala640Val(p.A640V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000262450
Start	6129060:6129060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3397C>T
AA Mutation	p.Arg1133Cys(p.R1133C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262450
Start	6155703:6155703(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775725361
CDS Mutation	c.402G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262450
Start	6155670:6155670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140138233
CDS Mutation	c.435C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262450
Start	6146818:6146818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1437G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262450
Start	6148911:6148911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1326C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262450
Start	6109895:6109895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200881726
CDS Mutation	c.5478C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262450
Start	6142152:6142152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2412T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262450
Start	6154721:6154721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768857681
CDS Mutation	c.684C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262450
Start	6124616:6124616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765484235
CDS Mutation	c.4440G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262450
Start	6149333:6149333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147670357
CDS Mutation	c.1074C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262450
Start	6111825:6111825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764640532
CDS Mutation	c.5199C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	37
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262450
Start	6109943:6109943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs191295192
CDS Mutation	c.5430G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	38
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262450
Start	6152466:6152466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140463225
CDS Mutation	c.816C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	39
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262450
Start	6146319:6146319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1695C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	40
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262450
Start	6152442:6152442(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.840delG
AA Mutation	p.Ile281SerfsTer185(p.I281Sfs*185)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	41
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262450
Start	6136633:6136633(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2580delT
AA Mutation	p.Phe860LeufsTer4(p.F860Lfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	42
Mutation Consequence	stop_gained
Transcription ID	ENST00000262450
Start	6142539:6142539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2110C>T
AA Mutation	p.Gln704Ter(p.Q704*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	43
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000262450
Start	6143930:6143930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1936G>T
AA Mutation	p.Glu646Ter(p.E646*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	44
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000262450
Start	6125234:6125234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4261-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript