Variant #0001038584 (NC_000011.9:g.64410192_64410197dup, NC_000011.9(NM_015080.3):c.3403+5502_3403+5507dup (NRXN2))

Chromosome 11
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.64410192_64410197dup
DNA change (hg38) -
Published as NRXN2(NM_138734.3):c.87_92dup (p.(Pro31_Pro32dup))
ISCN -
DB-ID NRXN2_000049
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +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     
NRXN2 NM_015080.3 ?/. - c.3403+5502_3403+5507dup r.(=) p.(=)


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