Variant #0000261201 (NC_000023.10:g.40450585C>G, ATP6AP2(NM_005765.2):c.268C>G)

Chromosome X
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.40450585C>G
DNA change (hg38) g.40591333C>G
Published as ATP6AP2(NM_005765.2):c.268C>G (p.P90A), ATP6AP2(NM_005765.3):c.268C>G (p.P90A)
ISCN -
DB-ID ATP6AP2_000017 See all 3 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 0.04347 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ATP6AP2 NM_005765.2 -/. - c.268C>G r.(?) p.(Pro90Ala)