Variant #0000523975 (NC_000005.9:g.126791300G>A, NC_000005.9(NM_032446.2):c.3232+1G>A (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.126791300G>A
DNA change (hg38) g.127455608G>A
Published as MEGF10(NM_001256545.1):c.3232+1G>A (p.?)
ISCN -
DB-ID MEGF10_000016
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-17 14:57:27 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MEGF10 NM_032446.2 ?/. - c.3232+1G>A r.spl? p.?


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