Variant #0000622052 (NC_000008.10:g.20054931_20054939dup, NM_001693.3:c.14_22dup (ATP6V1B2))

Chromosome 8
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.20054931_20054939dup
DNA change (hg38) g.20197420_20197428dup
Published as ATP6V1B2(NM_001693.4):c.14_22dupCGATGCGGG (p.A5_R7dup)
ISCN -
DB-ID ATP6V1B2_000008
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 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ATP6V1B2 NM_001693.3 ?/. - c.14_22dup r.(?) p.(Ala5_Arg7dup)


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