Variant #0000086602 (NC_000007.13:g.138417718A>G, NM_020632.2:c.1812T>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.138417718A>G
DNA change (hg38) g.138732973A>G
Published as C>T (H604H)
ISCN -
DB-ID ATP6V0A4_000010 See all 3 reported entries
Variant remarks ethnically matched controls
Reference PubMed: Smith 2000, Journal: Smith 2000
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency 0.68 controls
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.72917 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2015-12-18 13:35:01 +01:00 (CET)
Date last edited 2019-04-09 14:57:52 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ATP6V0A4 NM_020632.2 -/. 17 c.1812T>C r.(=) p.(His604=)


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