Variant #0000507604 (NC_000001.10:g.44437176G>A, NM_014652.3:c.*3822G>A (IPO13))

Chromosome 1
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.44437176G>A
DNA change (hg38) g.43971504G>A
Published as DPH2(NM_001319170.1):c.23G>A (p.R8H)
ISCN -
DB-ID ATP6V0B_000001
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) 3.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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     
DPH2 NM_001384.4 ?/. - c.602G>A r.(?) p.(Arg201His)
ATP6V0B NM_004047.3 ?/. - c.-3537G>A r.(?) p.(=)
IPO13 NM_014652.3 ?/. - c.*3822G>A r.(=) p.(=)


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