Mutation

Primary Site >> Stomach Cancer

Gene >> LIMD1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000273317
Start	45676941:45676941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140945464
CDS Mutation	c.1913A>G
AA Mutation	p.Asn638Ser(p.N638S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000273317
Start	45636219:45636219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1478A>C
AA Mutation	p.Tyr493Ser(p.Y493S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000273317
Start	45595517:45595517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.638G>T
AA Mutation	p.Gly213Val(p.G213V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000273317
Start	45595451:45595451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.572G>A
AA Mutation	p.Gly191Asp(p.G191D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000273317
Start	45672714:45672714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1666T>C
AA Mutation	p.Tyr556His(p.Y556H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000273317
Start	45596000:45596000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755410946
CDS Mutation	c.1121G>A
AA Mutation	p.Cys374Tyr(p.C374Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273317
Start	45596073:45596073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1194G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273317
Start	45595344:45595344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374578310
CDS Mutation	c.465G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273317
Start	45595563:45595563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.684T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273317
Start	45595644:45595644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.765C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000273317
Start	45595833:45595833(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.959delG
AA Mutation	p.Gly320ValfsTer6(p.G320Vfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript