Variant #0000982309 (NC_000017.10:g.12921016_12921019del, NM_014859.4:c.*27528_*27531del (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.12921016_12921019del
DNA change (hg38) -
Published as ELAC2(NM_018127.7):c.245+5_245+8del
ISCN -
DB-ID ARHGAP44_000021
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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARHGAP44 NM_014859.4 ?/. - c.*27528_*27531del r.(=) p.(=)
ELAC2 NM_018127.6 ?/. - c.245+5_245+8del r.spl? p.?


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