Mutation

Primary Site >> Stomach Cancer

Gene >> POMC

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264708
Start	25161488:25161488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.397C>T
AA Mutation	p.Arg133Cys(p.R133C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264708
Start	25164661:25164661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.112A>G
AA Mutation	p.Thr38Ala(p.T38A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264708
Start	25161479:25161479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.406A>G
AA Mutation	p.Lys136Glu(p.K136E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264708
Start	25161421:25161421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.464G>A
AA Mutation	p.Arg155His(p.R155H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264708
Start	25161205:25161205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.680G>A
AA Mutation	p.Arg227His(p.R227H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000264708
Start	25161140:25161140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761359264
CDS Mutation	c.745C>T
AA Mutation	p.Pro249Ser(p.P249S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000264708
Start	25164751:25164751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761386423
CDS Mutation	c.22C>T
AA Mutation	p.Arg8Cys(p.R8C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264708
Start	25164662:25164662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.111C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264708
Start	25161498:25161498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.387G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000264708
Start	25161309:25161310(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.561_575dupGGGAGATGGCCCCGA
AA Mutation	p.Glu187_Pro191dup(p.E187_P191dup)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript