Mutation

Primary Site >> Stomach Cancer

Gene >> POR

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000394893
Start	75984858:75984858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781961684
CDS Mutation	c.1148C>T
AA Mutation	p.Pro383Leu(p.P383L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000394893
Start	75979469:75979469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.256T>C
AA Mutation	p.Phe86Leu(p.F86L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000394893
Start	75983808:75983808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1018A>G
AA Mutation	p.Ile340Val(p.I340V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000394893
Start	75985094:75985094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1285C>T
AA Mutation	p.His429Tyr(p.H429Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394893
Start	75979501:75979501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.288G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394893
Start	75979525:75979525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782013891
CDS Mutation	c.312C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394893
Start	75986182:75986182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782715627
CDS Mutation	c.1839G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000394893
Start	75985133:75985133(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1329delC
AA Mutation	p.Ile444SerfsTer101(p.I444Sfs*101)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000394893
Start	75972426:75972429(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.206_209delAGAG
AA Mutation	p.Glu69AlafsTer7(p.E69Afs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000394893
Start	75979544:75979544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.331C>T
AA Mutation	p.Arg111Ter(p.R111*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript