Mutation

Primary Site >> Stomach Cancer

Gene >> PRKAR2B

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265717
Start	107153244:107153244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.911T>C
AA Mutation	p.Ile304Thr(p.I304T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265717
Start	107146375:107146375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.655G>T
AA Mutation	p.Gly219Trp(p.G219W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265717
Start	107146417:107146417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.697G>A
AA Mutation	p.Ala233Thr(p.A233T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265717
Start	107140857:107140857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.491C>T
AA Mutation	p.Ser164Phe(p.S164F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265717
Start	107159487:107159487(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1162T>A
AA Mutation	p.Cys388Ser(p.C388S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000265717
Start	107153178:107153178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.845T>G
AA Mutation	p.Phe282Cys(p.F282C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000265717
Start	107157300:107157300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1099G>A
AA Mutation	p.Ala367Thr(p.A367T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000265717
Start	107157285:107157285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1084G>A
AA Mutation	p.Ala362Thr(p.A362T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265717
Start	107146386:107146386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146903153
CDS Mutation	c.666C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265717
Start	107146342:107146343(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.624dupT
AA Mutation	p.Gly209TrpfsTer6(p.G209Wfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265717
Start	107159501:107159502(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1180dupA
AA Mutation	p.Arg394LysfsTer7(p.R394Kfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	12
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000265717
Start	107151025:107151025(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.843+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript