Variant #0000320784 (NC_000001.10:g.44685757C>G, NM_024066.1:c.*1473G>C (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.44685757C>G
DNA change (hg38) g.44220085C>G
Published as DMAP1(NM_001034023.1):c.1120C>G (p.(Leu374Val))
ISCN -
DB-ID DMAP1_000003
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DMAP1 NM_019100.4 ?/. - c.1120C>G r.(?) p.(Leu374Val)
ERI3 NM_024066.1 ?/. - c.*1473G>C r.(=) p.(=)


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