Variant #0000336074 (NC_000023.10:g.153042686G>A, NM_005393.2:c.4951G>A (PLXNB3))

Chromosome X
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.153042686G>A
DNA change (hg38) g.153777231G>A
Published as PLXNB3(NM_005393.3):c.4951G>A (p.(Glu1651Lys))
ISCN -
DB-ID PLXNB3_000064
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) 0.00091 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PLXNB3 NM_005393.2 -?/. - c.4951G>A r.(?) p.(Glu1651Lys)
SRPK3 NM_014370.3 -?/. - c.-3856G>A r.(?) p.(=)


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