Variant #0000856491 (NC_000023.10:g.1720175A>G, AKAP17A(NM_005088.2):c.1776A>G)

Chromosome X
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.1720175A>G
DNA change (hg38) -
Published as AKAP17A(NM_005088.2):c.1776A>G (p.G592=)
ISCN -
DB-ID AKAP17A_000024
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) 6.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:47:41 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ASMT NM_004043.2 -?/. - c.-68+5750A>G r.(=) p.(=)
AKAP17A NM_005088.2 -?/. - c.1776A>G r.(?) p.(Gly592=)