Variant #0000608069 (NC_000002.11:g.71163196dup, NM_001692.3:c.112dup (ATP6V1B1))

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.71163196dup
DNA change (hg38) g.70936066dup
Published as ATP6V1B1(NM_001692.4):c.112dupC (p.R38Pfs*45)
ISCN -
DB-ID ATP6V1B1_000033
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 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ATP6V1B1 NM_001692.3 +/. - c.112dup r.(?) p.(Arg38ProfsTer45)
VAX2 NM_012476.2 +/. - c.*2862dup r.(?) p.(=)


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