Mutation

Primary Site >> Stomach Cancer

Gene >> MYH9

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000216181
Start	36288827:36288827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373393111
CDS Mutation	c.4670G>A
AA Mutation	p.Arg1557Gln(p.R1557Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000216181
Start	36300915:36300915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2774A>T
AA Mutation	p.Glu925Val(p.E925V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000216181
Start	36293415:36293415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4009G>A
AA Mutation	p.Glu1337Lys(p.E1337K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000216181
Start	36318256:36318256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202023656
CDS Mutation	c.1178G>A
AA Mutation	p.Arg393His(p.R393H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000216181
Start	36318257:36318257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1177C>T
AA Mutation	p.Arg393Cys(p.R393C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000216181
Start	36285737:36285737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5195C>T
AA Mutation	p.Ala1732Val(p.A1732V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000216181
Start	36314237:36314237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1462G>C
AA Mutation	p.Glu488Gln(p.E488Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000216181
Start	36284506:36284506(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5489G>A
AA Mutation	p.Arg1830His(p.R1830H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000216181
Start	36288881:36288881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772323929
CDS Mutation	c.4616C>T
AA Mutation	p.Thr1539Met(p.T1539M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000216181
Start	36293400:36293400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147901502
CDS Mutation	c.4024C>T
AA Mutation	p.Arg1342Trp(p.R1342W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000216181
Start	36288846:36288846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4651A>G
AA Mutation	p.Thr1551Ala(p.T1551A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000216181
Start	36294126:36294126(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768022369
CDS Mutation	c.3803G>A
AA Mutation	p.Arg1268His(p.R1268H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000216181
Start	36327485:36327485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs576081279
CDS Mutation	c.494G>A
AA Mutation	p.Arg165Gln(p.R165Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000216181
Start	36294130:36294130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756528783
CDS Mutation	c.3799G>A
AA Mutation	p.Val1267Met(p.V1267M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000216181
Start	36318223:36318223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1211C>T
AA Mutation	p.Ala404Val(p.A404V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000216181
Start	36348957:36348957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.280G>A
AA Mutation	p.Glu94Lys(p.E94K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000216181
Start	36302626:36302626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760924443
CDS Mutation	c.2441G>A
AA Mutation	p.Arg814Gln(p.R814Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000216181
Start	36293346:36293346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs569649580
CDS Mutation	c.4078G>A
AA Mutation	p.Ala1360Thr(p.A1360T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000216181
Start	36288902:36288902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs11549910
CDS Mutation	c.4595A>G
AA Mutation	p.Gln1532Arg(p.Q1532R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000216181
Start	36284187:36284187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748946434
CDS Mutation	c.5671G>A
AA Mutation	p.Ala1891Thr(p.A1891T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000216181
Start	36304052:36304052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2333A>C
AA Mutation	p.Lys778Thr(p.K778T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000216181
Start	36326632:36326632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.548A>G
AA Mutation	p.Asn183Ser(p.N183S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000216181
Start	36286825:36286825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4954C>T
AA Mutation	p.Arg1652Cys(p.R1652C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000216181
Start	36349212:36349212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.25T>C
AA Mutation	p.Tyr9His(p.Y9H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000216181
Start	36288780:36288780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4717C>A
AA Mutation	p.Leu1573Met(p.L1573M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000216181
Start	36282744:36282744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781388651
CDS Mutation	c.5807G>A
AA Mutation	p.Arg1936Gln(p.R1936Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000216181
Start	36288744:36288744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149169068
CDS Mutation	c.4753A>C
AA Mutation	p.Lys1585Gln(p.K1585Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	missense_variant
Transcription ID	ENST00000216181
Start	36312200:36312200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1577C>T
AA Mutation	p.Ala526Val(p.A526V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	29
Mutation Consequence	missense_variant
Transcription ID	ENST00000216181
Start	36312094:36312094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1683G>T
AA Mutation	p.Gln561His(p.Q561H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	30
Mutation Consequence	missense_variant
Transcription ID	ENST00000216181
Start	36288367:36288367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145319741
CDS Mutation	c.4817C>T
AA Mutation	p.Ser1606Leu(p.S1606L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	31
Mutation Consequence	missense_variant
Transcription ID	ENST00000216181
Start	36318233:36318233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369581570
CDS Mutation	c.1201G>A
AA Mutation	p.Val401Ile(p.V401I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216181
Start	36299025:36299025(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2994A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216181
Start	36288384:36288384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201223994
CDS Mutation	c.4800C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216181
Start	36296932:36296932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778202463
CDS Mutation	c.3183C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216181
Start	36312211:36312211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145517108
CDS Mutation	c.1566G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216181
Start	36296866:36296866(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3249G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	37
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216181
Start	36284453:36284453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5542C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	38
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216181
Start	36294152:36294152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3777C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	39
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216181
Start	36302619:36302619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs113285582
CDS Mutation	c.2448C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	40
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000216181
Start	36294247:36294247(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3682delG
AA Mutation	p.Glu1228SerfsTer6(p.E1228Sfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	41
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000216181
Start	36305962:36305962(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2127delC
AA Mutation	p.Asn710ThrfsTer15(p.N710Tfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	42
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000216181
Start	36320299:36320299(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.933delC
AA Mutation	p.Gln313SerfsTer14(p.Q313Sfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	43
Mutation Consequence	stop_gained;frameshift_variant
Transcription ID	ENST00000216181
Start	36284437:36284438(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.5554_5557dupGATG
AA Mutation	p.Asp1853GlyfsTer2(p.D1853Gfs*2)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	44
Mutation Consequence	stop_gained
Transcription ID	ENST00000216181
Start	36296988:36296988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3127C>T
AA Mutation	p.Arg1043Ter(p.R1043*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	45
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000216181
Start	36341416:36341417(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.443dupC
AA Mutation	p.His149SerfsTer27(p.H149Sfs*27)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	46
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000216181
Start	36285656:36285656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5274+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	47
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000216181
Start	36300205:36300207(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2896_2898delAAG
AA Mutation	p.Lys966del(p.K966del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript