Variant #0000296497 (NC_000023.10:g.6069116T>C, NM_020742.2:c.392A>G (NLGN4X))
| Chromosome |
X |
| 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.6069116T>C |
| DNA change (hg38) |
g.6151075T>C |
| Published as |
NLGN4X(NM_001282145.1):c.392A>G (p.N131S), NLGN4X(NM_020742.2):c.392A>G (p.(Asn131Ser)), NLGN4X(NM_020742.4):c.392A>G (p.N131S) |
| ISCN |
- |
| DB-ID |
NLGN4X_000042 See all 4 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_Groningen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Groningen |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2021-09-17 14:40:49 +02:00 (CEST) |

Variant on transcripts
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