Variant #0000560298 (NC_000017.10:g.12899252C>T, NM_014859.4:c.*5764C>T (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.12899252C>T
DNA change (hg38) g.12995935C>T
Published as ELAC2(NM_001165962.1):c.1578+5G>A (p.?)
ISCN -
DB-ID ELAC2_000008
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-13 08:54:23 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARHGAP44 NM_014859.4 ?/. - c.*5764C>T r.(=) p.(=)
ELAC2 NM_018127.6 ?/. - c.1698+5G>A r.spl? p.?


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