Mutation

Primary Site >> Liver Cancer

Gene >> PCDHA6

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000529310
Start	140829772:140829772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1681A>T
AA Mutation	p.Asn561Tyr(p.N561Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000529310
Start	140828795:140828795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.704T>C
AA Mutation	p.Val235Ala(p.V235A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000529310
Start	140829970:140829970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1879T>C
AA Mutation	p.Tyr627His(p.Y627H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000529310
Start	140829617:140829617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1526C>T
AA Mutation	p.Ser509Leu(p.S509L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000529310
Start	140829965:140829965(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1874G>A
AA Mutation	p.Gly625Glu(p.G625E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000529310
Start	140829480:140829480(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781847846
CDS Mutation	c.1389C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000529310
Start	140829843:140829843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1752A>T
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000529310
Start	140828682:140828682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.591G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000529310
Start	140828931:140828931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.840T>A
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000529310
Start	140830464:140830464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2373A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000529310
Start	140828532:140828532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.441G>A
Mutation Classification	Silent
Feature Type	Transcript