Mutation

Primary Site >> Stomach Cancer

Gene >> MYH14

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376970
Start	50250681:50250681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764094116
CDS Mutation	c.1799C>T
AA Mutation	p.Ala600Val(p.A600V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000376970
Start	50249776:50249776(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1585G>A
AA Mutation	p.Asp529Asn(p.D529N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000376970
Start	50291037:50291037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764344864
CDS Mutation	c.4993C>T
AA Mutation	p.Arg1665Cys(p.R1665C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000376970
Start	50281657:50281657(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777626365
CDS Mutation	c.4231C>T
AA Mutation	p.Arg1411Trp(p.R1411W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000376970
Start	50217709:50217709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776632941
CDS Mutation	c.500G>A
AA Mutation	p.Arg167His(p.R167H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000376970
Start	50281829:50281829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760481743
CDS Mutation	c.4403G>A
AA Mutation	p.Arg1468His(p.R1468H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000376970
Start	50293568:50293568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5227G>T
AA Mutation	p.Ala1743Ser(p.A1743S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000376970
Start	50231963:50231963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.983G>A
AA Mutation	p.Arg328Gln(p.R328Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000376970
Start	50244305:50244305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1154A>G
AA Mutation	p.Asn385Ser(p.N385S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000376970
Start	50276780:50276780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200988515
CDS Mutation	c.3581C>T
AA Mutation	p.Thr1194Met(p.T1194M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000376970
Start	50210525:50210525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.160C>T
AA Mutation	p.Arg54Cys(p.R54C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000376970
Start	50301695:50301695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754861302
CDS Mutation	c.5381G>A
AA Mutation	p.Arg1794His(p.R1794H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000376970
Start	50249053:50249053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745888926
CDS Mutation	c.1372C>T
AA Mutation	p.Arg458Cys(p.R458C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000376970
Start	50261569:50261569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370936318
CDS Mutation	c.2396G>A
AA Mutation	p.Arg799Gln(p.R799Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000376970
Start	50244323:50244323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1172T>C
AA Mutation	p.Met391Thr(p.M391T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000376970
Start	50309041:50309041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5701C>T
AA Mutation	p.Arg1901Trp(p.R1901W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000376970
Start	50244310:50244310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771031207
CDS Mutation	c.1159G>A
AA Mutation	p.Asp387Asn(p.D387N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000376970
Start	50281673:50281673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs727503224
CDS Mutation	c.4247G>A
AA Mutation	p.Arg1416Gln(p.R1416Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000376970
Start	50217729:50217729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373197435
CDS Mutation	c.520G>A
AA Mutation	p.Val174Met(p.V174M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000376970
Start	50271443:50271443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770972513
CDS Mutation	c.2945C>T
AA Mutation	p.Ala982Val(p.A982V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000376970
Start	50301694:50301694(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751422907
CDS Mutation	c.5380C>T
AA Mutation	p.Arg1794Cys(p.R1794C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000376970
Start	50261481:50261481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2308G>A
AA Mutation	p.Ala770Thr(p.A770T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000376970
Start	50309641:50309641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747594595
CDS Mutation	c.5839C>T
AA Mutation	p.Arg1947Cys(p.R1947C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376970
Start	50231943:50231943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.963C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376970
Start	50217632:50217632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.423C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376970
Start	50250628:50250628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1746C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376970
Start	50261568:50261568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2395C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376970
Start	50261483:50261483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746902884
CDS Mutation	c.2310G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000376970
Start	50309646:50309646(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.5848delC
AA Mutation	p.Leu1950SerfsTer14(p.L1950Sfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	30
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000376970
Start	50231929:50231929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.950-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	31
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000376970
Start	50281615:50281616(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.4199_4201dupAGG
AA Mutation	p.Glu1400dup(p.E1400dup)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript