Mutation

Primary Site >> Stomach Cancer

Gene >> MECOM

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000468789
Start	169090069:169090069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2768A>T
AA Mutation	p.Glu923Val(p.E923V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000468789
Start	169084949:169084949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201825977
CDS Mutation	c.3116C>T
AA Mutation	p.Ala1039Val(p.A1039V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000468789
Start	169121182:169121182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150819501
CDS Mutation	c.442C>T
AA Mutation	p.Arg148Trp(p.R148W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000468789
Start	169121151:169121151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.473G>A
AA Mutation	p.Arg158Gln(p.R158Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000468789
Start	169121190:169121190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.434A>G
AA Mutation	p.Asn145Ser(p.N145S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000468789
Start	169115894:169115894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1414G>C
AA Mutation	p.Asp472His(p.D472H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000468789
Start	169131463:169131463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.15C>A
AA Mutation	p.Asp5Glu(p.D5E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000468789
Start	169115721:169115721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368981948
CDS Mutation	c.1587G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000494292
Start	169381361:169381361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.201C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000468789
Start	169115475:169115475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766090691
CDS Mutation	c.1833A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000468789
Start	169127891:169127891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150481592
CDS Mutation	c.219G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000468789
Start	169121105:169121105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.519G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000468789
Start	169115469:169115469(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs773080349
CDS Mutation	c.1839delA
AA Mutation	p.Gly614GlufsTer30(p.G614Efs*30)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000468789
Start	169090070:169090070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2767G>T
AA Mutation	p.Glu923Ter(p.E923*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000468789
Start	169115816:169115817(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1491dupA
AA Mutation	p.Val498SerfsTer27(p.V498Sfs*27)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	16
Mutation Consequence	splice_acceptor_variant;coding_sequence_variant
Transcription ID	ENST00000468789
Start	169100962:169100963(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2208-1_2208delGA
Mutation Classification	Splice_Site
Feature Type	Transcript