Mutation

Primary Site >> Stomach Cancer

Gene >> DYNC1H1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360184
Start	102027712:102027712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.9142G>A
AA Mutation	p.Glu3048Lys(p.E3048K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000360184
Start	102039093:102039093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.11299A>G
AA Mutation	p.Ile3767Val(p.I3767V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000360184
Start	102039430:102039430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.11479T>C
AA Mutation	p.Tyr3827His(p.Y3827H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000360184
Start	102010325:102010325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6271C>T
AA Mutation	p.Arg2091Trp(p.R2091W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000360184
Start	102012103:102012103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374569905
CDS Mutation	c.6847G>A
AA Mutation	p.Val2283Met(p.V2283M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000360184
Start	102050124:102050124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.13738G>A
AA Mutation	p.Ala4580Thr(p.A4580T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000360184
Start	101986350:101986350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2125C>T
AA Mutation	p.Arg709Cys(p.R709C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000360184
Start	102049793:102049793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.13595A>C
AA Mutation	p.Asn4532Thr(p.N4532T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000360184
Start	102040401:102040401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.11856G>T
AA Mutation	p.Gln3952His(p.Q3952H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000360184
Start	102017167:102017167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7928G>A
AA Mutation	p.Arg2643His(p.R2643H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000360184
Start	102027201:102027201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8799G>C
AA Mutation	p.Leu2933Phe(p.L2933F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000360184
Start	102012321:102012321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6865G>A
AA Mutation	p.Asp2289Asn(p.D2289N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000360184
Start	102005203:102005203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5400G>C
AA Mutation	p.Gln1800His(p.Q1800H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000360184
Start	102028052:102028052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.9379C>T
AA Mutation	p.Pro3127Ser(p.P3127S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000360184
Start	102039499:102039499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.11548A>G
AA Mutation	p.Thr3850Ala(p.T3850A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000360184
Start	101980524:101980524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.935C>T
AA Mutation	p.Ala312Val(p.A312V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000360184
Start	101987519:101987519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2605T>C
AA Mutation	p.Tyr869His(p.Y869H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000360184
Start	102001263:102001263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4304G>T
AA Mutation	p.Trp1435Leu(p.W1435L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000360184
Start	102008274:102008274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5914T>C
AA Mutation	p.Ser1972Pro(p.S1972P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000360184
Start	102017160:102017160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7921T>C
AA Mutation	p.Tyr2641His(p.Y2641H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000360184
Start	102029882:102029882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.9706G>A
AA Mutation	p.Ala3236Thr(p.A3236T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000360184
Start	102027679:102027679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769817685
CDS Mutation	c.9109G>A
AA Mutation	p.Ala3037Thr(p.A3037T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000360184
Start	102036571:102036571(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.10837A>G
AA Mutation	p.Ser3613Gly(p.S3613G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000360184
Start	101975717:101975717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.262G>A
AA Mutation	p.Val88Ile(p.V88I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000360184
Start	102009993:102009993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6128A>G
AA Mutation	p.Lys2043Arg(p.K2043R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000360184
Start	102027425:102027425(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8929C>T
AA Mutation	p.Arg2977Trp(p.R2977W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000360184
Start	101985931:101985931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1706G>A
AA Mutation	p.Arg569Gln(p.R569Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	missense_variant
Transcription ID	ENST00000360184
Start	102001191:102001191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4232G>A
AA Mutation	p.Arg1411His(p.R1411H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	29
Mutation Consequence	missense_variant
Transcription ID	ENST00000360184
Start	102012106:102012106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6850C>A
AA Mutation	p.Leu2284Met(p.L2284M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	30
Mutation Consequence	missense_variant
Transcription ID	ENST00000360184
Start	101991531:101991531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2873T>C
AA Mutation	p.Val958Ala(p.V958A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	31
Mutation Consequence	missense_variant
Transcription ID	ENST00000360184
Start	102049852:102049852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.13654A>G
AA Mutation	p.Thr4552Ala(p.T4552A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	32
Mutation Consequence	missense_variant
Transcription ID	ENST00000360184
Start	102027181:102027181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8779C>T
AA Mutation	p.Arg2927Cys(p.R2927C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	33
Mutation Consequence	missense_variant
Transcription ID	ENST00000360184
Start	101986386:101986386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2161G>A
AA Mutation	p.Glu721Lys(p.E721K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	34
Mutation Consequence	missense_variant
Transcription ID	ENST00000360184
Start	101975738:101975738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.283G>A
AA Mutation	p.Glu95Lys(p.E95K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	35
Mutation Consequence	missense_variant
Transcription ID	ENST00000360184
Start	102027746:102027746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.9176T>C
AA Mutation	p.Ile3059Thr(p.I3059T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	36
Mutation Consequence	missense_variant
Transcription ID	ENST00000360184
Start	101985772:101985772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1547A>G
AA Mutation	p.Asp516Gly(p.D516G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	37
Mutation Consequence	missense_variant
Transcription ID	ENST00000360184
Start	102002668:102002668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4674G>T
AA Mutation	p.Lys1558Asn(p.K1558N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	38
Mutation Consequence	missense_variant
Transcription ID	ENST00000360184
Start	102034428:102034428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.10730C>T
AA Mutation	p.Ala3577Val(p.A3577V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	39
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360184
Start	102004869:102004869(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5157G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	40
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360184
Start	102000081:102000081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3897G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	41
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360184
Start	102044486:102044486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.12897C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	42
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360184
Start	102049480:102049480(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776463183
CDS Mutation	c.13413C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	43
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360184
Start	102015143:102015143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7053G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	44
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360184
Start	101995255:101995255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3519G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	45
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360184
Start	102012411:102012411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6955C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	46
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360184
Start	102012335:102012335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748519888
CDS Mutation	c.6879C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	47
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360184
Start	102039643:102039643(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781162203
CDS Mutation	c.11601G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	48
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360184
Start	102039182:102039182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149806996
CDS Mutation	c.11388C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	49
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360184
Start	102050141:102050141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.13755T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	50
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360184
Start	101986673:101986673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145405293
CDS Mutation	c.2448C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	51
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000360184
Start	101979451:101979451(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.483delT
AA Mutation	p.Phe161LeufsTer52(p.F161Lfs*52)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	52
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000360184
Start	102010079:102010079(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.6219delT
AA Mutation	p.Phe2073LeufsTer21(p.F2073Lfs*21)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	53
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000360184
Start	102006099:102006099(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.5650delC
AA Mutation	p.Leu1884SerfsTer7(p.L1884Sfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	54
Mutation Consequence	stop_gained
Transcription ID	ENST00000360184
Start	102005213:102005213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5410C>T
AA Mutation	p.Arg1804Ter(p.R1804*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	55
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000360184
Start	102010078:102010079(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.6219dupT
AA Mutation	p.Lys2074Ter(p.K2074*)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	56
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000360184
Start	102039683:102039684(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.11643dupT
AA Mutation	p.Thr3882TyrfsTer32(p.T3882Yfs*32)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	57
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000360184
Start	102016927:102016928(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.7778dupT
AA Mutation	p.Leu2593PhefsTer22(p.L2593Ffs*22)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	58
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000360184
Start	102041572:102041572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.11942-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	59
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000360184
Start	102017119:102017121(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.7881_7883delTCC
AA Mutation	p.Pro2628del(p.P2628del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript