Mutation

Primary Site >> Stomach Cancer

Gene >> CYP11A1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000268053
Start	74367459:74367459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.127C>T
AA Mutation	p.Arg43Cys(p.R43C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000268053
Start	74348003:74348003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.322G>C
AA Mutation	p.Ala108Pro(p.A108P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000268053
Start	74339314:74339314(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1159C>A
AA Mutation	p.Leu387Ile(p.L387I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000268053
Start	74338002:74338002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1536G>T
AA Mutation	p.Trp512Cys(p.W512C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000268053
Start	74343104:74343104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.863T>C
AA Mutation	p.Leu288Ser(p.L288S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000268053
Start	74343804:74343804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750547647
CDS Mutation	c.814G>A
AA Mutation	p.Val272Met(p.V272M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268053
Start	74367484:74367484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.102T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268053
Start	74347959:74347959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs530494910
CDS Mutation	c.366C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268053
Start	74345180:74345180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.489C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000268053
Start	74343880:74343880(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.738delC
AA Mutation	p.Met247CysfsTer26(p.M247Cfs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000268053
Start	74339260:74339260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1213C>T
AA Mutation	p.Arg405Ter(p.R405*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript