Variant #0000990617 (NC_000001.10:g.183212479A>G, NM_005562.2:c.3526A>G (LAMC2))

Chromosome 1
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.183212479A>G
DNA change (hg38) -
Published as LAMC2(NM_005562.3):c.3526A>G (p.I1176V)
ISCN -
DB-ID LAMC2_000045
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) 0.00013 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-08-28 13:07:21 +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     
LAMC2 NM_005562.2 ?/. - c.3526A>G r.(?) p.(Ile1176Val)
NMNAT2 NM_015039.3 ?/. - c.*9297T>C r.(=) p.(=)


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