Mutation

Primary Site >> Stomach Cancer

Gene >> GFRA3

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000274721
Start	138253349:138253349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1051T>G
AA Mutation	p.Phe351Val(p.F351V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000274721
Start	138257790:138257790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.634G>A
AA Mutation	p.Ala212Thr(p.A212T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000274721
Start	138253037:138253037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1134G>C
AA Mutation	p.Arg378Ser(p.R378S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000274721
Start	138274363:138274363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.62T>C
AA Mutation	p.Leu21Pro(p.L21P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274721
Start	138264442:138264442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.198C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274721
Start	138264348:138264348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.292C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274721
Start	138257842:138257842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775939048
CDS Mutation	c.582C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274721
Start	138257800:138257800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754570944
CDS Mutation	c.624C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274721
Start	138257707:138257707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.717C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274721
Start	138257869:138257869(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.555G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	splice_donor_variant;coding_sequence_variant;intron_variant
Transcription ID	ENST00000274721
Start	138264248:138264261(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.379_379+13delGGTGAGGCTCCCAT
Mutation Classification	Splice_Site
Feature Type	Transcript