Variant #0001066382 (NC_000016.9:g.2569712G>T, NM_001694.3:c.434G>T (ATP6V0C))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.2569712G>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID AMDHD2_000003
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2026-01-20 18:57:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CEMP1 NM_001048212.3 +?/. - c.*10619C>A r.(=) p.(=)
ATP6V0C NM_001694.3 +?/. - c.434G>T r.(?) p.(Gly145Val)
AMDHD2 NM_015944.3 +?/. - c.-748G>T r.(?) p.(=)


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