Variant #0000254834 (NC_000012.11:g.124242557A>G, NM_207437.3:c.-4510A>G (DNAH10))

Chromosome 12
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.124242557A>G
DNA change (hg38) g.123758010A>G
Published as ATP6V0A2(NM_012463.3):c.2549A>G (p.N850S)
ISCN -
DB-ID ATP6V0A2_000033 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) 0.01112 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ATP6V0A2 NM_012463.3 -?/. - c.2549A>G r.(?) p.(Asn850Ser)
DNAH10 NM_207437.3 -?/. - c.-4510A>G r.(?) p.(=)


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