Mutation

Primary Site >> Stomach Cancer

Gene >> MYLK

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360304
Start	123700841:123700841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs537224715
CDS Mutation	c.2627G>A
AA Mutation	p.Arg876His(p.R876H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000360304
Start	123640424:123640424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757766496
CDS Mutation	c.4700G>A
AA Mutation	p.Arg1567Gln(p.R1567Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000360304
Start	123700323:123700323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3145C>T
AA Mutation	p.Pro1049Ser(p.P1049S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000360304
Start	123700095:123700095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3373C>G
AA Mutation	p.Pro1125Ala(p.P1125A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000360304
Start	123700811:123700811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140989388
CDS Mutation	c.2657C>T
AA Mutation	p.Ala886Val(p.A886V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000360304
Start	123708706:123708706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs531232445
CDS Mutation	c.2132C>T
AA Mutation	p.Thr711Met(p.T711M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000360304
Start	123666344:123666344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3706A>C
AA Mutation	p.Met1236Leu(p.M1236L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000360304
Start	123700501:123700501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2967G>T
AA Mutation	p.Lys989Asn(p.K989N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000360304
Start	123708782:123708782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2056T>C
AA Mutation	p.Phe686Leu(p.F686L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000360304
Start	123725964:123725964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146724203
CDS Mutation	c.1631G>A
AA Mutation	p.Arg544Gln(p.R544Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000360304
Start	123700563:123700563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2905G>A
AA Mutation	p.Glu969Lys(p.E969K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000360304
Start	123657329:123657329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4085C>A
AA Mutation	p.Ala1362Asp(p.A1362D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000360304
Start	123638110:123638110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4922C>T
AA Mutation	p.Ala1641Val(p.A1641V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000360304
Start	123638137:123638137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4895T>C
AA Mutation	p.Val1632Ala(p.V1632A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000360304
Start	123640299:123640299(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4825G>A
AA Mutation	p.Ala1609Thr(p.A1609T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000360304
Start	123614272:123614272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757115211
CDS Mutation	c.5578G>A
AA Mutation	p.Asp1860Asn(p.D1860N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000360304
Start	123664174:123664174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755117377
CDS Mutation	c.3916G>A
AA Mutation	p.Gly1306Ser(p.G1306S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000360304
Start	123700226:123700226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs113491038
CDS Mutation	c.3242A>G
AA Mutation	p.His1081Arg(p.H1081R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000360304
Start	123657261:123657261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373683421
CDS Mutation	c.4153C>T
AA Mutation	p.Arg1385Cys(p.R1385C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000360304
Start	123614292:123614292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375758782
CDS Mutation	c.5558G>A
AA Mutation	p.Arg1853His(p.R1853H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000360304
Start	123620332:123620332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5243C>T
AA Mutation	p.Thr1748Met(p.T1748M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000360304
Start	123664189:123664189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368321325
CDS Mutation	c.3901C>T
AA Mutation	p.Arg1301Cys(p.R1301C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000360304
Start	123657134:123657134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4280A>C
AA Mutation	p.Lys1427Thr(p.K1427T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000360304
Start	123700758:123700758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2710A>C
AA Mutation	p.Lys904Gln(p.K904Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000360304
Start	123752420:123752420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.284C>T
AA Mutation	p.Ala95Val(p.A95V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360304
Start	123700786:123700786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2682G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360304
Start	123752473:123752473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.231C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360304
Start	123700729:123700729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs530064548
CDS Mutation	c.2739C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360304
Start	123647340:123647340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4503A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360304
Start	123734147:123734147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758274846
CDS Mutation	c.849G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360304
Start	123682228:123682228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3648T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360304
Start	123640333:123640333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775517621
CDS Mutation	c.4791G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360304
Start	123640468:123640468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749367561
CDS Mutation	c.4656C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360304
Start	123733988:123733988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143682943
CDS Mutation	c.1008G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	35
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000360304
Start	123657413:123657413(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4001delC
AA Mutation	p.Pro1334GlnfsTer15(p.P1334Qfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	36
Mutation Consequence	stop_gained
Transcription ID	ENST00000360304
Start	123614119:123614119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5731G>T
AA Mutation	p.Glu1911Ter(p.E1911*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	37
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000360304
Start	123626892:123626893(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.5163dupA
AA Mutation	p.Asp1722ArgfsTer68(p.D1722Rfs*68)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	38
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000360304
Start	123739012:123739013(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.472dupG
AA Mutation	p.Glu158GlyfsTer54(p.E158Gfs*54)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	39
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000360304
Start	123666336:123666337(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.3713dupC
AA Mutation	p.Gln1239SerfsTer7(p.Q1239Sfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript