Variant #0000576884 (NC_000023.10:g.63005007C>T, NM_001173479.1:c.19G>A (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.63005007C>T
DNA change (hg38) g.63785127C>T
Published as ARHGEF9(NM_001173479.1):c.19G>A (p.G7R)
ISCN -
DB-ID ARHGEF9_000031
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +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.19G>A r.(?) p.(Gly7Arg)
ARHGEF9 NM_015185.2 ?/. - c.-30815G>A r.(?) p.(=)


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