Variant #0000342921 (NC_000007.13:g.138430000C>T, NM_020632.2:c.1346G>A (ATP6V0A4))

Chromosome 7
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.138430000C>T
DNA change (hg38) g.138745255C>T
Published as -
ISCN -
DB-ID ATP6V0A4_000025
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TMEM213 NM_001085429.1 +?/. - c.-52850C>T r.(?) p.(=)
ATP6V0A4 NM_020632.2 +?/. - c.1346G>A r.(?) p.(Arg449His)


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