Variant #0000859720 (NC_000005.9:g.126791085C>T, NC_000005.9(NM_032446.2):c.3026-8C>T (MEGF10))

Chromosome 5
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.126791085C>T
DNA change (hg38) -
Published as MEGF10(NM_001256545.1):c.3026-8C>T (p.(=)), MEGF10(NM_032446.2):c.3026-8C>T
ISCN -
DB-ID MEGF10_000005 See all 2 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) 0.00156 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 2022-05-09 15:51:19 +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     
MEGF10 NM_032446.2 -?/. - c.3026-8C>T r.(=) p.(=)


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