Mutation

Primary Site >> Stomach Cancer

Gene >> MED1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000300651
Start	39409262:39409262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759693158
CDS Mutation	c.2959G>A
AA Mutation	p.Gly987Arg(p.G987R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000300651
Start	39410527:39410527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1694A>T
AA Mutation	p.Asn565Ile(p.N565I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000300651
Start	39409408:39409408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2813G>A
AA Mutation	p.Gly938Asp(p.G938D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000300651
Start	39408992:39408992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3229C>T
AA Mutation	p.Pro1077Ser(p.P1077S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000300651
Start	39407818:39407818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4403G>A
AA Mutation	p.Gly1468Asp(p.G1468D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000300651
Start	39409000:39409000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3221T>C
AA Mutation	p.Val1074Ala(p.V1074A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000300651
Start	39410534:39410534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs1139822
CDS Mutation	c.1687C>T
AA Mutation	p.Pro563Ser(p.P563S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000300651
Start	39415131:39415131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1394T>C
AA Mutation	p.Val465Ala(p.V465A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300651
Start	39408426:39408426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3795C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300651
Start	39408042:39408042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4179C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300651
Start	39415257:39415257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1380C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300651
Start	39410439:39410439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1782C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300651
Start	39408477:39408477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780589147
CDS Mutation	c.3744G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300651
Start	39408471:39408471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3750A>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000300651
Start	39409723:39409723(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2498delA
AA Mutation	p.Asn833IlefsTer31(p.N833Ifs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000300651
Start	39407846:39407846(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4375delC
AA Mutation	p.Gln1459ArgfsTer13(p.Q1459Rfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	17
Mutation Consequence	stop_gained;frameshift_variant
Transcription ID	ENST00000300651
Start	39408751:39408752(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.3469_3470insAGGGAAGATGA
AA Mutation	p.Pro1157GlnfsTer4(p.P1157Qfs*4)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000300651
Start	39407693:39407694(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.4527_4528insCCAATCAT
AA Mutation	p.Lys1510ProfsTer40(p.K1510Pfs*40)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000300651
Start	39408752:39408753(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.3468_3469insTCCTCATCTGCTTCCACCT
AA Mutation	p.Pro1157SerfsTer18(p.P1157Sfs*18)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript