Variant #0000682611 (NC_000023.10:g.70389799C>T, NM_018977.3:c.2339C>T (NLGN3))

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.70389799C>T
DNA change (hg38) -
Published as NLGN3(NM_181303.1):c.2399C>T (p.P800L), NLGN3(NM_181303.2):c.2399C>T (p.P800L)
ISCN -
DB-ID NLGN3_000038 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) 2.0E-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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2022-05-09 15:24:52 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NLGN3 NM_018977.3 ?/. - c.2339C>T r.(?) p.(Pro780Leu)


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