Variant #0000553189 (NC_000014.8:g.80327663_80327664del, NC_000014.8(NM_001105250.2):c.1079-343_1079-342del (NRXN3))

Chromosome 14
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.80327663_80327664del
DNA change (hg38) g.79861320_79861321del
Published as NRXN3(NM_001272020.1):c.1268_1269del (p.(Thr424HisfsTer8))
ISCN -
DB-ID NRXN3_000015
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NRXN3 NM_001105250.2 ?/. - c.1079-343_1079-342del r.(=) p.(=)


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