Mutation

Primary Site >> Stomach Cancer

Gene >> CNR1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369499
Start	88144049:88144049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143455045
CDS Mutation	c.1226G>A
AA Mutation	p.Arg409Gln(p.R409Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369499
Start	88144955:88144955(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.320G>T
AA Mutation	p.Cys107Phe(p.C107F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369499
Start	88144343:88144343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777110971
CDS Mutation	c.932G>A
AA Mutation	p.Arg311His(p.R311H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000369499
Start	88144615:88144615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.660G>T
AA Mutation	p.Arg220Ser(p.R220S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000369499
Start	88144266:88144266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773478911
CDS Mutation	c.1009A>G
AA Mutation	p.Met337Val(p.M337V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000369499
Start	88143875:88143875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138027855
CDS Mutation	c.1400C>T
AA Mutation	p.Thr467Met(p.T467M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000369499
Start	88144533:88144533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768033952
CDS Mutation	c.742G>A
AA Mutation	p.Ala248Thr(p.A248T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000369499
Start	88144833:88144833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.442C>T
AA Mutation	p.Arg148Cys(p.R148C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000369499
Start	88144019:88144019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs78783387
CDS Mutation	c.1256C>T
AA Mutation	p.Ala419Val(p.A419V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000369499
Start	88144145:88144145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764560714
CDS Mutation	c.1130C>T
AA Mutation	p.Thr377Met(p.T377M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369499
Start	88144630:88144630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.645C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369499
Start	88144606:88144606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.669C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369499
Start	88144666:88144666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.609C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369499
Start	88144060:88144060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1215A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369499
Start	88145122:88145122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.153T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369499
Start	88144669:88144669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.606C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369499
Start	88144873:88144874(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.401dupA
AA Mutation	p.Asn134LysfsTer43(p.N134Kfs*43)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript