Variant #0000320782 (NC_000001.10:g.44684917C>T, NM_024066.1:c.*2313G>A (ERI3))

Chromosome 1
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.44684917C>T
DNA change (hg38) g.44219245C>T
Published as DMAP1(NM_001034023.1):c.906+4C>T (p.?)
ISCN -
DB-ID DMAP1_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) 9.0E-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 2020-06-04 13:09:51 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DMAP1 NM_019100.4 ?/. - c.906+4C>T r.spl? p.?
ERI3 NM_024066.1 ?/. - c.*2313G>A r.(=) p.(=)


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