Variant #0000803278 (NC_000007.13:g.91737906G>A, NM_005751.4:c.11645G>A (AKAP9))

Chromosome 7
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.91737906G>A
DNA change (hg38) -
Published as AKAP9(NM_005751.5):c.11645G>A (p.R3882Q)
ISCN -
DB-ID AKAP9_000326
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 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
CYP51A1 NM_000786.3 ?/. - c.*5073C>T r.(=) p.(=) -
AKAP9 NM_005751.4 ?/. - c.11645G>A r.(?) p.(Arg3882Gln) -


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