Variant #0000983199 (NC_000019.9:g.1244112C>T, NM_001687.4:c.312C>T (ATP5D))

Chromosome 19
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.1244112C>T
DNA change (hg38) -
Published as ATP5F1D(NM_001687.5):c.312C>T (p.(Ile104=))
ISCN -
DB-ID ATP5D_000006
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) 0.00395 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ATP5D NM_001687.4 -/. - c.312C>T r.(?) p.(=)
MIDN NM_177401.4 -/. - c.-4955C>T r.(?) p.(=)


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