Variant #0001064397 (NC_000005.9:g.126774253A>G, NM_001256545.2:c.2227A>G (MEGF10))

Chromosome 5
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.126774253A>G
DNA change (hg38) g.127438561A>G
Published as MEGF10(NM_001256545.2):c.2227A>G (p.(Thr743Ala))
ISCN -
DB-ID MEGF10_000048
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 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 2026-01-20 18:57:21 +01:00 (CET)
Date last edited 2026-04-11 09:10:45 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MEGF10 NM_001256545.2 ?/. - c.2227A>G r.(?) p.(Thr743Ala)


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