Variant #0000338648 (NC_000002.11:g.71163220C>T, NC_000002.11(NM_001692.3):c.118+18C>T (ATP6V1B1))

Chromosome 2
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.71163220C>T
DNA change (hg38) g.70936090C>T
Published as -
ISCN -
DB-ID ATP6V1B1_000017
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) 0.02829 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ATP6V1B1 NM_001692.3 -/. - c.118+18C>T r.(=) p.(=)
VAX2 NM_012476.2 -/. - c.*2886C>T r.(=) p.(=)


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