Variant #0000326511 (NC_000019.9:g.41281790C>T, NM_053046.3:c.-23988C>T (EGLN2))

Chromosome 19
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.41281790C>T
DNA change (hg38) g.40775885C>T
Published as MIA(NM_001202553.1):c.261C>T (p.?)
ISCN -
DB-ID MIA_000001
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) 2.0E-5 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-15 18:41:47 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MIA NM_001202553.1 ?/. - c.261C>T r.(?) p.(Ser87=)
RAB4B NM_016154.4 ?/. - c.-2491C>T r.(?) p.(=)
EGLN2 NM_053046.3 ?/. - c.-23988C>T r.(?) p.(=)
MIA-RAB4B NR_037775.1 ?/. - n.267C>T r.(?) -


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