Variant #0000507605 (NC_000001.10:g.44437728C>T, NM_014652.3:c.*4374C>T (IPO13))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.44437728C>T
DNA change (hg38) g.43972056C>T
Published as DPH2(NM_001319170.1):c.575C>T (p.A192V)
ISCN -
DB-ID ATP6V0B_000002
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) 4.0E-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.1154C>T r.(?) p.(Ala385Val)
ATP6V0B NM_004047.3 -?/. - c.-2985C>T r.(?) p.(=)
IPO13 NM_014652.3 -?/. - c.*4374C>T r.(=) p.(=)


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