Variant #0001006530 (NC_000023.10:g.153047285T>G, NM_005393.2:c.*2791T>G (PLXNB3))

Chromosome X
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.153047285T>G
DNA change (hg38) -
Published as SRPK3(NM_014370.3):c.387T>G (p.C129W, p.(Cys129Trp))
ISCN -
DB-ID SRPK3_000015 See all 2 reported entries
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) 1.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +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     
IDH3G NM_004135.3 ?/. - c.*4042A>C r.(=) p.(=)
PLXNB3 NM_005393.2 ?/. - c.*2791T>G r.(=) p.(=)
SRPK3 NM_014370.3 ?/. - c.387T>G r.(?) p.(Cys129Trp)


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