Variant #0000616344 (NC_000017.10:g.12906855_12906858dup, NM_014859.4:c.*13367_*13370dup (ARHGAP44))

Chromosome 17
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.12906855_12906858dup
DNA change (hg38) g.13003538_13003541dup
Published as ELAC2(NM_001165962.1):c.901_902insGTGG (p.(Val301GlyfsTer25))
ISCN -
DB-ID ELAC2_000015
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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2021-02-08 18:36:18 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARHGAP44 NM_014859.4 ?/. - c.*13367_*13370dup r.(=) p.(=)
ELAC2 NM_018127.6 ?/. - c.1018_1021dup r.(?) p.(Val341GlyfsTer25)


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