Variant #0001013248 (NC_000001.10:g.183197677C>A, NM_005562.2:c.1637C>A (LAMC2))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.183197677C>A
DNA change (hg38) -
Published as LAMC2(NM_005562.2):c.1637C>A (p.A546D), LAMC2(NM_005562.3):c.1637C>A (p.(Ala546Asp), p.A546D)
ISCN -
DB-ID LAMC2_000040 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) 0.00177 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 2024-10-29 20:49:11 +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     
LAMC2 NM_005562.2 -?/. - c.1637C>A r.(?) p.(Ala546Asp)


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