Mutation

Primary Site >> Stomach Cancer

Gene >> ADAM33

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356518
Start	3672798:3672798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755851229
CDS Mutation	c.1234G>A
AA Mutation	p.Gly412Arg(p.G412R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356518
Start	3673444:3673444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1043G>A
AA Mutation	p.Gly348Asp(p.G348D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356518
Start	3672307:3672307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1424G>A
AA Mutation	p.Cys475Tyr(p.C475Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000356518
Start	3672305:3672305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779669835
CDS Mutation	c.1426C>T
AA Mutation	p.Arg476Cys(p.R476C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000356518
Start	3674235:3674235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.650T>C
AA Mutation	p.Val217Ala(p.V217A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000356518
Start	3669367:3669367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2336C>A
AA Mutation	p.Pro779His(p.P779H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356518
Start	3672829:3672829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749815451
CDS Mutation	c.1203C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356518
Start	3672877:3672877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1155C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356518
Start	3672830:3672830(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1202delG
AA Mutation	p.Gly401AlafsTer68(p.G401Afs*68)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	10
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000356518
Start	3672628:3672628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1312-2A>C
Mutation Classification	Splice_Site
Feature Type	Transcript