Variant #0000895402 (NC_000020.10:g.60897778T>C, NM_005560.4:c.6101A>G (LAMA5))

Chromosome 20
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.60897778T>C
DNA change (hg38) -
Published as LAMA5(NM_005560.3):c.6101A>G (p.(Asp2034Gly))
ISCN -
DB-ID LAMA5_000070
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 5.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2022-11-01 13:41:49 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LAMA5 NM_005560.4 ?/. - c.6101A>G r.(?) p.(Asp2034Gly)


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