Variant #0000290774 (NC_000009.11:g.133914570G>A, NM_006059.3:c.1218G>A (LAMC3))

Chromosome 9
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.133914570G>A
DNA change (hg38) g.131039183G>A
Published as LAMC3(NM_006059.3):c.1218G>A (p.T406=), LAMC3(NM_006059.4):c.1218G>A (p.T406=)
ISCN -
DB-ID LAMC3_000006 See all 3 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) 0.21305 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LAMC3 NM_006059.3 -/. - c.1218G>A r.(?) p.(Thr406=)


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