Mutation

Primary Site >> Stomach Cancer

Gene >> RUNX2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371438
Start	45512318:45512318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749565421
CDS Mutation	c.932C>T
AA Mutation	p.Thr311Met(p.T311M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371438
Start	45512272:45512272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.886C>T
AA Mutation	p.Pro296Ser(p.P296S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371438
Start	45547289:45547289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1550T>C
AA Mutation	p.Val517Ala(p.V517A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000371438
Start	45438030:45438030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.664G>C
AA Mutation	p.Asp222His(p.D222H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000371438
Start	45546982:45546982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1243A>G
AA Mutation	p.Thr415Ala(p.T415A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000371438
Start	45547022:45547022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1283G>A
AA Mutation	p.Gly428Asp(p.G428D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000371438
Start	45437973:45437973(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147009083
CDS Mutation	c.607G>A
AA Mutation	p.Val203Ile(p.V203I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371438
Start	45547224:45547224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377403216
CDS Mutation	c.1485C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371438
Start	45437972:45437972(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776247579
CDS Mutation	c.606C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371438
Start	45422867:45422867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.333C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371438
Start	45422618:45422618(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.90delC
AA Mutation	p.Ser31ProfsTer9(p.S31Pfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	12
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000371438
Start	45422718:45422729(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.195_206delACAGCAGCAGCA
AA Mutation	p.Gln68_Gln71del(p.Q68_Q71del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript