Variant #0000929602 (NC_000009.11:g.35658038_35658039insGCTTCACAGAGTAGT, NM_001216.2:c.-15919_-15918insGCTTCACAGAGTAGT (CA9))

Chromosome 9
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.35658038_35658039insGCTTCACAGAGTAGT
DNA change (hg38) -
Published as RMRP(NR_003051.3):n.-24_-23insACTACTCTGTGAAGC
ISCN -
DB-ID CA9_000025
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-07-07 10:10:56 +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.-15919_-15918insGCTTCACAGAGTAGT r.(?) p.(=)
ARHGEF39 NM_032818.2 +/. - c.*3945_*3946insACTACTCTGTGAAGC r.(=) p.(=)
CCDC107 NM_174923.2 +/. - c.-339_-338insGCTTCACAGAGTAGT r.(?) p.(=)


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