Variant #0000970928 (NC_000023.10:g.153662651A>G, NM_001183.4:c.782A>G (ATP6AP1))

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.153662651A>G
DNA change (hg38) -
Published as ATP6AP1(NM_001183.6):c.782A>G (p.N261S)
ISCN -
DB-ID GDI1_000038
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) 1.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-02-26 20:06:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ATP6AP1 NM_001183.4 ?/. - c.782A>G r.(?) p.(Asn261Ser)
GDI1 NM_001493.2 ?/. - c.-2950A>G r.(?) p.(=)


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