Mutation

Primary Site >> Stomach Cancer

Gene >> DIAPH2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000324765
Start	96912392:96912392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.652G>A
AA Mutation	p.Asp218Asn(p.D218N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000324765
Start	96916556:96916556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.851T>G
AA Mutation	p.Ile284Ser(p.I284S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000324765
Start	96758244:96758244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.433G>A
AA Mutation	p.Ala145Thr(p.A145T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000324765
Start	97072971:97072971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2081A>C
AA Mutation	p.Lys694Thr(p.K694T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000324765
Start	96957940:96957940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1727C>A
AA Mutation	p.Pro576His(p.P576H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000324765
Start	97114922:97114922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2546G>A
AA Mutation	p.Arg849Lys(p.R849K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000324765
Start	96881669:96881669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.538C>A
AA Mutation	p.Leu180Ile(p.L180I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000324765
Start	97247820:97247820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2825A>C
AA Mutation	p.Lys942Thr(p.K942T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324765
Start	96758171:96758171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200157443
CDS Mutation	c.360C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324765
Start	96957917:96957917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757187745
CDS Mutation	c.1704G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324765
Start	97099738:97099738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2292A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324765
Start	96738747:96738747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.327C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000324765
Start	96738622:96738622(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.207delA
AA Mutation	p.Glu70LysfsTer15(p.E70Kfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000324765
Start	96937242:96937243(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1104dupA
AA Mutation	p.Glu369ArgfsTer3(p.E369Rfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	15
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000324765
Start	96958150:96958150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1935+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript