Variant #0000933451 (NC_000018.9:g.21501018G>A, NM_198129.1:c.8043G>A (LAMA3))

Chromosome 18
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.21501018G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID LAMA3_000037 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1002717654
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2023-09-17 22:05:01 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LAMA3 NM_198129.1 +?/. - c.8043G>A r.(?) p.(Ser2681=)


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