Mutation

Primary Site >> Stomach Cancer

Gene >> ADARB1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360697
Start	45220992:45220992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752123605
CDS Mutation	c.2024G>A
AA Mutation	p.Arg675His(p.R675H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000360697
Start	45182629:45182629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1123A>G
AA Mutation	p.Thr375Ala(p.T375A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000360697
Start	45176581:45176581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.880G>A
AA Mutation	p.Ala294Thr(p.A294T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000360697
Start	45185036:45185036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757268939
CDS Mutation	c.1630G>A
AA Mutation	p.Gly544Arg(p.G544R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000360697
Start	45176396:45176396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.695G>T
AA Mutation	p.Ser232Ile(p.S232I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000360697
Start	45204563:45204563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1694T>C
AA Mutation	p.Val565Ala(p.V565A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000360697
Start	45204677:45204677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1808G>A
AA Mutation	p.Arg603Gln(p.R603Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000360697
Start	45184947:45184947(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780427333
CDS Mutation	c.1541G>A
AA Mutation	p.Arg514His(p.R514H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000360697
Start	45182715:45182715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1209G>T
AA Mutation	p.Leu403Phe(p.L403F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000360697
Start	45184995:45184995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770534585
CDS Mutation	c.1589C>T
AA Mutation	p.Thr530Met(p.T530M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000360697
Start	45175945:45175945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.244G>A
AA Mutation	p.Ala82Thr(p.A82T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360697
Start	45176211:45176211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs574341919
CDS Mutation	c.510C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360697
Start	45171662:45171662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360697
Start	45183485:45183485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1371C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000360697
Start	45222143:45222143(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2176delG
AA Mutation	p.Ala726ProfsTer121(p.A726Pfs*121)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	16
Mutation Consequence	splice_donor_variant;coding_sequence_variant;intron_variant
Transcription ID	ENST00000360697
Start	45180439:45180449(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1075_1078+7delACAGGTAACCA
Mutation Classification	Splice_Site
Feature Type	Transcript