Mutation

Primary Site >> Stomach Cancer

Gene >> PDLIM5

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000317968
Start	94575829:94575829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761636570
CDS Mutation	c.505G>A
AA Mutation	p.Val169Ile(p.V169I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000317968
Start	94657455:94657455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762186735
CDS Mutation	c.1493G>C
AA Mutation	p.Trp498Ser(p.W498S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000317968
Start	94575694:94575694(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757010684
CDS Mutation	c.370G>A
AA Mutation	p.Ala124Thr(p.A124T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000317968
Start	94455332:94455332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.44G>A
AA Mutation	p.Gly15Asp(p.G15D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000317968
Start	94618054:94618054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs115018620
CDS Mutation	c.971G>A
AA Mutation	p.Arg324Gln(p.R324Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000317968
Start	94657440:94657440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763438199
CDS Mutation	c.1478C>T
AA Mutation	p.Ala493Val(p.A493V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317968
Start	94585655:94585655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.801T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317968
Start	94654544:94654544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1368T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317968
Start	94654613:94654613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1437T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000317968
Start	94618171:94618172(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1089_1091dupGCA
AA Mutation	p.Gln364dup(p.Q364dup)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript