Variant #0000516426 (NC_000002.11:g.50574047G>A, NC_000002.11(NM_001135659.1):c.3485-109939C>T (NRXN1))

Chromosome 2
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.50574047G>A
DNA change (hg38) g.50346909G>A
Published as NRXN1(NM_001330092.1):c.41C>T (p.S14L), NRXN1(NM_138735.2):c.41C>T (p.(Ser14Leu))
ISCN -
DB-ID NRXN1_000054 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) 0.00063 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NRXN1 NM_001135659.1 ?/. - c.3485-109939C>T r.(=) p.(=)


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