Variant #0000039755 (NC_000014.8:g.23243710dup, NM_001126105.2:c.1098dup (SLC7A7))
| Chromosome |
14 |
| Allele |
Both (homozygous) |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Probably affects function |
| Classification method |
- |
| Clinical classification |
likely pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.23243710dup |
| DNA change (hg38) |
g.22774501dup |
| Published as |
c.1099insT, p.Ile367TyrfsX16 |
| ISCN |
- |
| DB-ID |
SLC7A7_000057 |
| Variant remarks |
2 Turkish patients (hom) with LPI |
| Reference |
PubMed: Güzel-Ozantürk et al. 2013 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
yes |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Anne Polvi |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Anne Polvi |
| Date created |
2014-07-26 16:59:19 +02:00 (CEST) |
| Date last edited |
2020-07-04 15:16:49 +02:00 (CEST) |

Variant on transcripts
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