Variant #0000996227 (NC_000007.13:g.138424359T>C, NM_020632.2:c.1498A>G (ATP6V0A4))

Chromosome 7
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.138424359T>C
DNA change (hg38) -
Published as ATP6V0A4(NM_020632.3):c.1498A>G (p.S500G)
ISCN -
DB-ID ATP6V0A4_000053
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) 0.00242 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
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     
TMEM213 NM_001085429.1 -?/. - c.-58491T>C r.(?) p.(=)
ATP6V0A4 NM_020632.2 -?/. - c.1498A>G r.(?) p.(Ser500Gly)


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