Variant #0000896315 (NC_000023.10:g.62893915T>C, NC_000023.10(NM_001173479.1):c.765+3A>G (ARHGEF9))

Chromosome X
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.62893915T>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID ARHGEF9_000042
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2022-11-01 13:41:49 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARHGEF9 NM_001173479.1 ?/. - c.765+3A>G r.spl? p.?
ARHGEF9 NM_015185.2 ?/. - c.924+3A>G r.spl? p.?


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