Variant #0001006587 (NC_000023.10:g.153663679G>A, NM_001183.4:c.1031G>A (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.153663679G>A
DNA change (hg38) -
Published as ATP6AP1(NM_001183.4):c.1031G>A (p.(Arg344His)), ATP6AP1(NM_001183.5):c.1031G>A (p.R344H)
ISCN -
DB-ID GDI1_000022 See all 2 reported entries
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +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     
ATP6AP1 NM_001183.4 ?/. - c.1031G>A r.(?) p.(Arg344His)
GDI1 NM_001493.2 ?/. - c.-1922G>A r.(?) p.(=)


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