Variant #0000321778 (NC_000010.10:g.119303011dup, NM_004098.3:c.233dup (EMX2))

Chromosome 10
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.119303011dup
DNA change (hg38) g.117543500dup
Published as EMX2(NM_001165924.1):c.233dup (p.(Pro79Alafs*59))
ISCN -
DB-ID EMX2_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) 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 2022-05-09 15:51:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EMX2 NM_004098.3 -?/. - c.233dup r.(?) p.(Pro79AlafsTer62)
EMX2OS NR_002791.2 -?/. - n.574+808dup r.(?) -


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