Variant #0000982307 (NC_000017.10:g.12909099C>T, NM_014859.4:c.*15611C>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.12909099C>T
DNA change (hg38) -
Published as ELAC2(NM_018127.7):c.841G>A (p.(Gly281Arg))
ISCN -
DB-ID ARHGAP44_000019
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) 4.0E-5 View details
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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARHGAP44 NM_014859.4 ?/. - c.*15611C>T r.(=) p.(=)
ELAC2 NM_018127.6 ?/. - c.841G>A r.(?) p.(Gly281Arg)


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