Mutation

Primary Site >> Stomach Cancer

Gene >> MAP3K10

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000253055
Start	40212870:40212870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763193956
CDS Mutation	c.1618C>T
AA Mutation	p.Arg540Cys(p.R540C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000253055
Start	40204564:40204564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750540519
CDS Mutation	c.943G>A
AA Mutation	p.Val315Met(p.V315M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000253055
Start	40206028:40206028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1306C>T
AA Mutation	p.Arg436Trp(p.R436W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000253055
Start	40192467:40192467(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.436G>T
AA Mutation	p.Ala146Ser(p.A146S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000253055
Start	40206124:40206124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1402C>T
AA Mutation	p.Arg468Trp(p.R468W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000253055
Start	40198477:40198477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.785G>A
AA Mutation	p.Ser262Asn(p.S262N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253055
Start	40215139:40215139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs565611295
CDS Mutation	c.2712C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000253055
Start	40209173:40209173(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1511delC
AA Mutation	p.Pro504LeufsTer10(p.P504Lfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000253055
Start	40212921:40212921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1669C>T
AA Mutation	p.Arg557Ter(p.R557*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000253055
Start	40206158:40206158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1435+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript