Mutation

Primary Site >> Liver Cancer

Gene >> ADCY8

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000286355
Start	130836311:130836311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2641T>C
AA Mutation	p.Phe881Leu(p.F881L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000286355
Start	130884672:130884672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2001T>G
AA Mutation	p.Ile667Met(p.I667M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000286355
Start	130785427:130785427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3109G>A
AA Mutation	p.Gly1037Ser(p.G1037S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000286355
Start	130849660:130849660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781040718
CDS Mutation	c.2354G>A
AA Mutation	p.Arg785Gln(p.R785Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000286355
Start	130943389:130943389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1315C>T
AA Mutation	p.Leu439Phe(p.L439F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000286355
Start	131039537:131039537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.797T>G
AA Mutation	p.Leu266Arg(p.L266R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000286355
Start	130884581:130884581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2092T>C
AA Mutation	p.Ser698Pro(p.S698P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000286355
Start	131039877:131039877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.457A>T
AA Mutation	p.Ile153Phe(p.I153F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286355
Start	130785392:130785392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3144T>A
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286355
Start	130903931:130903931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1752T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286355
Start	130884687:130884687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1986T>A
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286355
Start	131039770:131039770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs80098122
CDS Mutation	c.564G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286355
Start	130849662:130849662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2352C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286355
Start	130937189:130937189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1365C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286355
Start	130836435:130836435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2517G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000286355
Start	130821347:130821347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2749C>T
AA Mutation	p.Gln917Ter(p.Q917*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000286355
Start	130780755:130780755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3391C>T
AA Mutation	p.Gln1131Ter(p.Q1131*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript