Variant #0000887689 (NC_000007.13:g.138453918G>A, NM_020632.2:c.196C>T (ATP6V0A4))

Chromosome 7
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.138453918G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID ATP6V0A4_000051
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) 3.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited 2025-07-08 13:22:38 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TMEM213 NM_001085429.1 ?/. - c.-28932G>A r.(?) p.(=)
ATP6V0A4 NM_020632.2 ?/. - c.196C>T r.(?) p.(Arg66Cys)


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