Variant #0001006895 (NC_000023.10:g.62917025C>T, NM_001173479.1:c.382G>A (ARHGEF9))

Chromosome X
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.62917025C>T
DNA change (hg38) -
Published as ARHGEF9(NM_015185.3):c.541G>A (p.G181R)
ISCN -
DB-ID ARHGEF9_000047
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2024-08-28 13:16:32 +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     
ARHGEF9 NM_001173479.1 +?/. - c.382G>A r.(?) p.(Gly128Arg)
ARHGEF9 NM_015185.2 +?/. - c.541G>A r.(?) p.(Gly181Arg)


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