Mutation

Primary Site >> Liver Cancer

Gene >> PCDH7

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000511884
Start	30920222:30920222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2313T>A
AA Mutation	p.Cys772Ser(p.C772S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361762
Start	30722650:30722650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1228G>A
AA Mutation	p.Asp410Asn(p.D410N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361762
Start	30723196:30723196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1774C>A
AA Mutation	p.Leu592Met(p.L592M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361762
Start	30722890:30722890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1468T>C
AA Mutation	p.Ser490Pro(p.S490P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000511884
Start	31142806:31142806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2770C>T
AA Mutation	p.Pro924Leu(p.P924L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000361762
Start	30730753:30730753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3175A>T
AA Mutation	p.Met1059Leu(p.M1059L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000361762
Start	30721646:30721646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.224T>A
AA Mutation	p.Leu75Gln(p.L75Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000361762
Start	30723622:30723622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2200G>T
AA Mutation	p.Asp734Tyr(p.D734Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000361762
Start	30722510:30722510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1088C>T
AA Mutation	p.Thr363Met(p.T363M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000361762
Start	30723288:30723288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1866C>A
AA Mutation	p.Ser622Arg(p.S622R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000361762
Start	30723783:30723783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2361T>A
AA Mutation	p.Asn787Lys(p.N787K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000361762
Start	30724404:30724404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370196952
CDS Mutation	c.2982G>T
AA Mutation	p.Arg994Ser(p.R994S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000361762
Start	30722373:30722373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.951G>T
AA Mutation	p.Leu317Phe(p.L317F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361762
Start	30722130:30722130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.708C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361762
Start	30724416:30724416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2994T>A
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361762
Start	30722685:30722685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1263G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000511884
Start	30920332:30920332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2423G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000511884
Start	30920152:30920152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2244-1G>C
Mutation Classification	Splice_Site
Feature Type	Transcript