Variant #0000969787 (NC_000019.9:g.42852466G>A, NC_000019.9(NM_001410.2):c.2098-1185G>A (MEGF8))

Chromosome 19
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.42852466G>A
DNA change (hg38) -
Published as MEGF8(NM_001271938.1):c.2140G>A (p.(Ala714Thr))
ISCN -
DB-ID MEGF8_000108
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) 0.00015 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 2024-02-26 20:06:56 +01:00 (CET)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MEGF8 NM_001271938.1 -?/. - c.2140G>A r.(?) p.(Ala714Thr)
MEGF8 NM_001410.2 -?/. - c.2098-1185G>A r.(=) p.(=)


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