Variant #0000621097 (NC_000002.11:g.51253512_51253513del, NM_001135659.1:c.868_869del (NRXN1))

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.51253512_51253513del
DNA change (hg38) g.51026374_51026375del
Published as NRXN1(NM_001135659.2):c.868_869delGA (p.E290Kfs*18), NRXN1(NM_001135659.3):c.868_869delGA (p.E290Kfs*18)
ISCN -
DB-ID NRXN1_000068 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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NRXN1 NM_001135659.1 +/. - c.868_869del r.(?) p.(Glu290LysfsTer18)


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