Mutation

Primary Site >> Stomach Cancer

Gene >> AMOT

ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000371959
Start	112791832:112791832(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1926G>T
AA Mutation	p.Gln642His(p.Q642H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371959
Start	112815574:112815574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772179248
CDS Mutation	c.1176A>C
AA Mutation	p.Gln392His(p.Q392H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371959
Start	112790684:112790684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2025A>C
AA Mutation	p.Glu675Asp(p.E675D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000371959
Start	112811308:112811308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1478T>C
AA Mutation	p.Met493Thr(p.M493T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000371959
Start	112811374:112811374(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1412G>A
AA Mutation	p.Arg471His(p.R471H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000371959
Start	112790631:112790631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2078A>C
AA Mutation	p.His693Pro(p.H693P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000371959
Start	112780996:112780996(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2363T>C
AA Mutation	p.Leu788Pro(p.L788P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000371959
Start	112805038:112805038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139517376
CDS Mutation	c.1685G>A
AA Mutation	p.Arg562His(p.R562H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000371959
Start	112779656:112779656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773540622
CDS Mutation	c.2498G>A
AA Mutation	p.Arg833His(p.R833H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000371959
Start	112782603:112782603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762949054
CDS Mutation	c.2177G>A
AA Mutation	p.Arg726His(p.R726H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000371959
Start	112811288:112811288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745879297
CDS Mutation	c.1498G>A
AA Mutation	p.Glu500Lys(p.E500K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371959
Start	112791949:112791949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1809G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371959
Start	112811349:112811349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs184493349
CDS Mutation	c.1437C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371959
Start	112790600:112790600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2109T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371959
Start	112815385:112815401(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1349_1365delAAGAGTTGGAAGGATGC
AA Mutation	p.Gln450LeufsTer2(p.Q450Lfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000371959
Start	112791870:112791870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1888C>T
AA Mutation	p.Arg630Ter(p.R630*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript