Variant #0000800744 (NC_000002.11:g.50779909T>C, NM_001135659.1:c.1695A>G (NRXN1))

Chromosome 2
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.50779909T>C
DNA change (hg38) -
Published as NRXN1(NM_001135659.2):c.1695A>G (p.R565=), NRXN1(NM_004801.5):c.1575A>G (p.R525=)
ISCN -
DB-ID NRXN1_000069 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) 0.00046 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 2021-09-17 14:40:49 +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     
NRXN1 NM_001135659.1 -?/. - c.1695A>G r.(?) p.(Arg565=)


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