Variant #0001056953 (NC_000020.10:g.60888201G>A, NM_005560.4:c.8898C>T (LAMA5))

Chromosome 20
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.60888201G>A
DNA change (hg38) -
Published as LAMA5(NM_005560.4):c.8898C>T (p.F2966=), LAMA5(NM_005560.6):c.8898C>T (p.(Phe2966=))
ISCN -
DB-ID ADRM1_000026 See all 2 reported entries
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) 0.00338 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 2025-11-01 13:22:20 +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     
ADRM1 NM_001281437.1 -/. - c.*4384G>A r.(=) p.(=)
LAMA5 NM_005560.4 -/. - c.8898C>T r.(?) p.(Phe2966=)


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