Mutation

Primary Site >> Stomach Cancer

Gene >> MYO9A

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356056
Start	71826800:71826800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7427G>A
AA Mutation	p.Gly2476Asp(p.G2476D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356056
Start	71854523:71854523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747452822
CDS Mutation	c.6200G>A
AA Mutation	p.Arg2067His(p.R2067H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356056
Start	71878147:71878147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751012778
CDS Mutation	c.5824C>T
AA Mutation	p.Arg1942Cys(p.R1942C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000356056
Start	72021006:72021006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1010T>C
AA Mutation	p.Val337Ala(p.V337A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000356056
Start	72010407:72010407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1196T>G
AA Mutation	p.Phe399Cys(p.F399C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000356056
Start	71951861:71951861(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2218A>C
AA Mutation	p.Ser740Arg(p.S740R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000356056
Start	72045761:72045761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.803T>C
AA Mutation	p.Val268Ala(p.V268A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000356056
Start	71897483:71897483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5020A>C
AA Mutation	p.Lys1674Gln(p.K1674Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000356056
Start	71897731:71897731(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4772C>T
AA Mutation	p.Ser1591Phe(p.S1591F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000356056
Start	72046155:72046155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.409C>T
AA Mutation	p.Arg137Trp(p.R137W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000356056
Start	71862571:71862571(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760390220
CDS Mutation	c.6020A>G
AA Mutation	p.Tyr2007Cys(p.Y2007C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000356056
Start	71899791:71899791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201961799
CDS Mutation	c.3366A>G
AA Mutation	p.Ile1122Met(p.I1122M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000356056
Start	71826656:71826656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199960921
CDS Mutation	c.7571G>A
AA Mutation	p.Arg2524His(p.R2524H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000356056
Start	71904008:71904008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2798T>C
AA Mutation	p.Leu933Pro(p.L933P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000356056
Start	71898100:71898100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4403G>A
AA Mutation	p.Cys1468Tyr(p.C1468Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356056
Start	71898543:71898543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3960T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356056
Start	72046068:72046068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.496C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356056
Start	71960022:71960022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2061T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356056
Start	71898239:71898239(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.4264delT
AA Mutation	p.Tyr1422IlefsTer8(p.Y1422Ifs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356056
Start	71897941:71897942(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4561_4562delGA
AA Mutation	p.Asp1521TyrfsTer13(p.D1521Yfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	21
Mutation Consequence	stop_gained;protein_altering_variant
Transcription ID	ENST00000356056
Start	71898226:71898227(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.4276_4277insTGAAATAGTTCAATGAGAATTATCTAGTGA
AA Mutation	p.Gln1426delinsLeuLysTerPheAsnGluAsnTyrLeuValLys(p.Q1426delinsLK*FNENYLVK)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	stop_gained
Transcription ID	ENST00000356056
Start	71935435:71935435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2428A>T
AA Mutation	p.Arg810Ter(p.R810*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356056
Start	71898224:71898225(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.4278_4279insT
AA Mutation	p.Asp1427Ter(p.D1427*)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript