Variant #0000251124 (NC_000007.13:g.138417791A>G, NM_020632.2:c.1739T>C (ATP6V0A4))

Chromosome 7
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.138417791A>G
DNA change (hg38) g.138733046A>G
Published as ATP6V0A4(NM_020632.3):c.1739T>C (p.M580T)
ISCN -
DB-ID ATP6V0A4_000005 See all 2 reported entries
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) 0.06546 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TMEM213 NM_001085429.1 -/. - c.-65059A>G r.(?) p.(=)
ATP6V0A4 NM_020632.2 -/. - c.1739T>C r.(?) p.(Met580Thr)


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