Mutation

Primary Site >> Stomach Cancer

Gene >> MYO5A

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000399231
Start	52397333:52397333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1187C>T
AA Mutation	p.Ala396Val(p.A396V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000399231
Start	52375443:52375443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs561485938
CDS Mutation	c.2438G>T
AA Mutation	p.Arg813Leu(p.R813L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000399231
Start	52410351:52410351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.738A>T
AA Mutation	p.Lys246Asn(p.K246N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000399231
Start	52397235:52397235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1285C>A
AA Mutation	p.Gln429Lys(p.Q429K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000399231
Start	52376431:52376431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2336G>T
AA Mutation	p.Gly779Val(p.G779V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000399231
Start	52397412:52397412(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1108G>A
AA Mutation	p.Glu370Lys(p.E370K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000399231
Start	52397258:52397258(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1262A>G
AA Mutation	p.Gln421Arg(p.Q421R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000399231
Start	52376366:52376366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376727710
CDS Mutation	c.2401C>T
AA Mutation	p.Arg801Trp(p.R801W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000399231
Start	52351406:52351406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3697A>G
AA Mutation	p.Ser1233Gly(p.S1233G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000399231
Start	52372317:52372317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2624G>A
AA Mutation	p.Gly875Asp(p.G875D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000399231
Start	52397321:52397321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1199G>A
AA Mutation	p.Arg400His(p.R400H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000399231
Start	52433249:52433249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.64T>C
AA Mutation	p.Trp22Arg(p.W22R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000399231
Start	52376399:52376399(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2368C>T
AA Mutation	p.Arg790Trp(p.R790W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000399231
Start	52370257:52370257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2978C>T
AA Mutation	p.Ala993Val(p.A993V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000399231
Start	52319297:52319297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4922T>C
AA Mutation	p.Val1641Ala(p.V1641A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000399231
Start	52376476:52376476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2291A>G
AA Mutation	p.Asp764Gly(p.D764G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000399231
Start	52376452:52376452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs185892206
CDS Mutation	c.2315G>A
AA Mutation	p.Arg772Gln(p.R772Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399231
Start	52370301:52370301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2934G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399231
Start	52384197:52384197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1878A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399231
Start	52396331:52396331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1386G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399231
Start	52314174:52314174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5364A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399231
Start	52407359:52407359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.879T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000399231
Start	52387874:52387875(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1706_1707delAA
AA Mutation	p.Lys569ArgfsTer5(p.K569Rfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000399231
Start	52327861:52327861(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4626delA
AA Mutation	p.Val1543TyrfsTer2(p.V1543Yfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000399231
Start	52323386:52323386(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4694delT
AA Mutation	p.Leu1565CysfsTer4(p.L1565Cfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	26
Mutation Consequence	stop_gained
Transcription ID	ENST00000399231
Start	52330449:52330449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4384C>T
AA Mutation	p.Arg1462Ter(p.R1462*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	stop_gained
Transcription ID	ENST00000399231
Start	52379850:52379850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2071C>T
AA Mutation	p.Arg691Ter(p.R691*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000399231
Start	52370419:52370419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2818-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript