Mutation

Primary Site >> Stomach Cancer

Gene >> NLRP6

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000312165
Start	280920:280920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1186A>G
AA Mutation	p.Thr396Ala(p.T396A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000312165
Start	281443:281443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768823068
CDS Mutation	c.1709G>A
AA Mutation	p.Arg570His(p.R570H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000312165
Start	281721:281721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1987G>A
AA Mutation	p.Val663Met(p.V663M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000312165
Start	281325:281325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1591C>T
AA Mutation	p.Arg531Cys(p.R531C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000312165
Start	279866:279866(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.343G>A
AA Mutation	p.Val115Met(p.V115M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000312165
Start	279855:279855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.332C>T
AA Mutation	p.Thr111Met(p.T111M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000312165
Start	280981:280981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762893596
CDS Mutation	c.1247C>T
AA Mutation	p.Thr416Met(p.T416M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312165
Start	281297:281297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774885098
CDS Mutation	c.1563C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312165
Start	281195:281195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1461C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312165
Start	280967:280967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1233G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312165
Start	284631:284631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2529G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000312165
Start	280951:280951(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1219delG
AA Mutation	p.Asp407ThrfsTer21(p.D407Tfs*21)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	13
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000312165
Start	278599:278599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.29+1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript