Variant #0001033450 (NC_000002.11:g.71192125C>G, NM_001692.3:c.1416C>G (ATP6V1B1))

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.71192125C>G
DNA change (hg38) -
Published as ATP6V1B1(NM_001692.4):c.1416C>G (p.D472E, p.(Asp472Glu))
ISCN -
DB-ID ATP6V1B1_000032 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 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 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ATP6V1B1 NM_001692.3 ?/. - c.1416C>G r.(?) p.(Asp472Glu)


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