Mutation

Primary Site >> Stomach Cancer

Gene >> PTGER4

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302472
Start	40692148:40692148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1237A>C
AA Mutation	p.Asn413His(p.N413H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000302472
Start	40691960:40691960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769375242
CDS Mutation	c.1049G>A
AA Mutation	p.Arg350His(p.R350H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000302472
Start	40692005:40692005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1094A>G
AA Mutation	p.Asp365Gly(p.D365G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000302472
Start	40681532:40681532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.539C>T
AA Mutation	p.Ala180Val(p.A180V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000302472
Start	40681382:40681382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.389A>G
AA Mutation	p.Tyr130Cys(p.Y130C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000302472
Start	40681831:40681831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.838G>A
AA Mutation	p.Val280Met(p.V280M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000302472
Start	40681766:40681766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.773G>A
AA Mutation	p.Arg258Gln(p.R258Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000302472
Start	40692112:40692112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1201C>G
AA Mutation	p.Leu401Val(p.L401V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000302472
Start	40681635:40681635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773573829
CDS Mutation	c.642C>A
AA Mutation	p.His214Gln(p.H214Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302472
Start	40681530:40681530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.537G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000302472
Start	40692346:40692363(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1439_1456delCACTGAACTTATCAGAAA
AA Mutation	p.Thr480_Glu485del(p.T480_E485del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript