Mutation

Primary Site >> Stomach Cancer

Gene >> KREMEN1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000407188
Start	29094363:29094363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.197A>G
AA Mutation	p.Tyr66Cys(p.Y66C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000407188
Start	29137576:29137576(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.860G>A
AA Mutation	p.Arg287His(p.R287H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000407188
Start	29137353:29137353(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369566037
CDS Mutation	c.637G>A
AA Mutation	p.Ala213Thr(p.A213T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000407188
Start	29137635:29137635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762595574
CDS Mutation	c.919C>T
AA Mutation	p.Arg307Cys(p.R307C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000407188
Start	29137423:29137423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs571815008
CDS Mutation	c.707C>T
AA Mutation	p.Thr236Met(p.T236M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000407188
Start	29138758:29138758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1093A>G
AA Mutation	p.Ser365Gly(p.S365G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000407188
Start	29098877:29098877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763716781
CDS Mutation	c.270C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000407188
Start	29142091:29142091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1401C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000407188
Start	29121419:29121419(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.412delA
AA Mutation	p.Thr138ArgfsTer142(p.T138Rfs*142)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	10
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000407188
Start	29138835:29138835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1168+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript