Variant #0000263308 (NC_000012.11:g.124242471del, NM_207437.3:c.-4596del (DNAH10))

Chromosome 12
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.124242471del
DNA change (hg38) g.123757924del
Published as ATP6V0A2(NM_012463.3):c.2466-3delT, ATP6V0A2(NM_012463.4):c.2466-3delT
ISCN -
DB-ID ATP6V0A2_000031 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) Retrieve
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 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     
ATP6V0A2 NM_012463.3 -/. - c.2466-3del r.spl? p.?
DNAH10 NM_207437.3 -/. - c.-4596del r.(?) p.(=)


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