Variant #0000729097 (NC_000023.10:g.62857950T>A, NM_001173479.1:c.1350A>T (ARHGEF9))

Chromosome X
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.62857950T>A
DNA change (hg38) -
Published as ARHGEF9(NM_015185.2):c.1509A>T (p.P503=), ARHGEF9(NM_015185.3):c.1509A>T (p.P503=)
ISCN -
DB-ID ARHGEF9_000037 See all 2 reported entries
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) 0.00015 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARHGEF9 NM_001173479.1 -?/. - c.1350A>T r.(?) p.(Pro450=)
ARHGEF9 NM_015185.2 -?/. - c.1509A>T r.(?) p.(Pro503=)


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