Mutation

Primary Site >> Liver Cancer

Gene >> LAMA2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000421865
Start	129502750:129502750(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8336A>T
AA Mutation	p.Asp2779Val(p.D2779V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000421865
Start	129315888:129315888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758134778
CDS Mutation	c.3862G>A
AA Mutation	p.Val1288Ile(p.V1288I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000421865
Start	129267211:129267211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2314G>A
AA Mutation	p.Glu772Lys(p.E772K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000421865
Start	129402460:129402460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5699T>C
AA Mutation	p.Leu1900Ser(p.L1900S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000421865
Start	129342391:129342391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4360G>C
AA Mutation	p.Gly1454Arg(p.G1454R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000421865
Start	129250200:129250200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1871T>C
AA Mutation	p.Met624Thr(p.M624T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000421865
Start	129147046:129147046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.907A>T
AA Mutation	p.Asn303Tyr(p.N303Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000421865
Start	129270683:129270683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147744763
CDS Mutation	c.2382C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000421865
Start	129177791:129177791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1392G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000421865
Start	129297795:129297795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2967T>A
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000421865
Start	129315634:129315634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3714A>T
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000421865
Start	129491961:129491961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7959G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000421865
Start	129383158:129383158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4996C>T
AA Mutation	p.Gln1666Ter(p.Q1666*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript