Mutation

Primary Site >> Stomach Cancer

Gene >> PLCD1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000334661
Start	38009706:38009706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1393G>A
AA Mutation	p.Ala465Thr(p.A465T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000334661
Start	38009741:38009741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1358G>A
AA Mutation	p.Gly453Asp(p.G453D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000334661
Start	38010478:38010478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752737739
CDS Mutation	c.875G>A
AA Mutation	p.Arg292His(p.R292H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000334661
Start	38008097:38008097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777711868
CDS Mutation	c.2102G>A
AA Mutation	p.Arg701His(p.R701H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000334661
Start	38008477:38008477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372093444
CDS Mutation	c.1883G>A
AA Mutation	p.Arg628Gln(p.R628Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000334661
Start	38011653:38011653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780533634
CDS Mutation	c.449G>A
AA Mutation	p.Arg150Gln(p.R150Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000334661
Start	38011420:38011420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.584C>A
AA Mutation	p.Ser195Tyr(p.S195Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334661
Start	38010032:38010032(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1159C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334661
Start	38020270:38020270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.117G>A
Mutation Classification	Silent
Feature Type	Transcript