Variant #0000516425 (NC_000002.11:g.50574034_50574039dup, NC_000002.11(NM_001135659.1):c.3485-109906_3485-109901dup (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.50574034_50574039dup |
DNA change (hg38) |
g.50346896_50346901dup |
Published as |
NRXN1(NM_001330091.2):c.74_79dup (p.(Gly25_Gly26dup)), NRXN1(NM_001330092.2):c.74_79dupGCGGCG (p.G25_G26dup) |
ISCN |
- |
DB-ID |
NRXN1_000053 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 International |
Created by |
VKGL-NL_Groningen |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2025-05-05 21:14:00 +02:00 (CEST) |

Variant on transcripts
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