Variant #0001037512 (NC_000009.11:g.35665029C>T, NM_001216.2:c.-8928C>T (CA9))

Chromosome 9
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.35665029C>T
DNA change (hg38) -
Published as ARHGEF39(NM_032818.3):c.138G>A (p.(Thr46=))
ISCN -
DB-ID CA9_000033
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) 0.00055 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 2025-05-05 21:14:00 +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     
CA9 NM_001216.2 ?/. - c.-8928C>T r.(?) p.(=)
ARHGEF39 NM_032818.2 ?/. - c.138G>A r.(?) p.(=)
CCDC107 NM_174923.2 ?/. - c.*3845C>T r.(=) p.(=)


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