Variant #0001043478 (NC_000020.10:g.60888474C>G, NM_005560.4:c.8701G>C (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.60888474C>G
DNA change (hg38) -
Published as LAMA5(NM_005560.6):c.8701G>C (p.(Glu2901Gln))
ISCN -
DB-ID ADRM1_000060
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ADRM1 NM_001281437.1 ?/. - c.*4657C>G r.(=) p.(=)
LAMA5 NM_005560.4 ?/. - c.8701G>C r.(?) p.(Glu2901Gln)


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