Variant #0001044234 (NC_000023.10:g.1752119A>T, NM_005088.2:c.*31632A>T (AKAP17A))

Chromosome X
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.1752119A>T
DNA change (hg38) -
Published as ASMT(NM_001171038.2):c.723A>T (p.(Glu241Asp))
ISCN -
DB-ID AKAP17A_000027
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_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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ASMT NM_004043.2 ?/. - c.723A>T r.(?) p.(Glu241Asp)
AKAP17A NM_005088.2 ?/. - c.*31632A>T r.(=) p.(=)


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