Variant #0000856961 (NC_000001.10:g.150116873A>C, NC_000001.10(NM_007259.3):c.1626-14A>C (VPS45))

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.150116873A>C
DNA change (hg38) -
Published as VPS45(NM_007259.4):c.1626-14A>C
ISCN -
DB-ID PLEKHO1_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) 0.00058 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
VPS45 NM_007259.3 -?/. - c.1626-14A>C r.(=) p.(=)
PLEKHO1 NM_016274.4 -?/. - c.-5575A>C r.(?) p.(=)


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