Variant #0000260251 (NC_000007.13:g.138432309del, NM_020632.2:c.1185del (ATP6V0A4))

Chromosome 7
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.138432309del
DNA change (hg38) g.138747564del
Published as ATP6V0A4(NM_020632.3):c.1185delC (p.Y396Tfs*12)
ISCN -
DB-ID ATP6V0A4_000016
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) Retrieve
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +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.-50541del r.(?) p.(=)
ATP6V0A4 NM_020632.2 +/. - c.1185del r.(?) p.(Tyr396ThrfsTer12)


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