Mutation

Primary Site >> Stomach Cancer

Gene >> MAP3K7

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369329
Start	90548159:90548159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.968C>T
AA Mutation	p.Ala323Val(p.A323V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369329
Start	90544615:90544615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1228C>T
AA Mutation	p.Arg410Trp(p.R410W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369329
Start	90571726:90571726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.202G>A
AA Mutation	p.Glu68Lys(p.E68K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000369329
Start	90560148:90560148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.410G>A
AA Mutation	p.Cys137Tyr(p.C137Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000369329
Start	90519317:90519317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1465A>G
AA Mutation	p.Thr489Ala(p.T489A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000369329
Start	90516646:90516646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1676A>G
AA Mutation	p.Lys559Arg(p.K559R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000369329
Start	90523706:90523706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1434T>A
AA Mutation	p.Ser478Arg(p.S478R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000369329
Start	90553521:90553521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.673C>T
AA Mutation	p.Arg225Cys(p.R225C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000369329
Start	90544561:90544561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147070999
CDS Mutation	c.1282G>A
AA Mutation	p.Val428Ile(p.V428I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369329
Start	90560198:90560198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.360A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	splice_acceptor_variant;coding_sequence_variant;intron_variant
Transcription ID	ENST00000369329
Start	90561661:90561673(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.298-6_304delCTTTAGGTGTGTC
Mutation Classification	Splice_Site
Feature Type	Transcript