Variant #0000336251 (NC_000023.10:g.153696236G>A, NM_017514.3:c.3712G>A (PLXNA3))

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.153696236G>A
DNA change (hg38) g.154467893G>A
Published as PLXNA3(NM_017514.3):c.3712G>A (p.(Val1238Met)), PLXNA3(NM_017514.4):c.3712G>A (p.V1238M)
ISCN -
DB-ID PLXNA3_000001 See all 3 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) 0.00052 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 2019-12-04 15:24:38 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PLXNA3 NM_017514.3 ?/. - c.3712G>A r.(?) p.(Val1238Met)


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