Variant #0001037510 (NC_000009.11:g.35658003T>C, NM_001216.2:c.-15954T>C (CA9))

Chromosome 9
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.35658003T>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID CA9_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) 2.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited 2025-11-01 13:22:20 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CA9 NM_001216.2 +?/. - c.-15954T>C r.(?) p.(=)
ARHGEF39 NM_032818.2 +?/. - c.*3981A>G r.(=) p.(=)
CCDC107 NM_174923.2 +?/. - c.-374T>C r.(?) p.(=)


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