Variant #0000016699 (NC_000014.8:g.23249134C>G, NC_000014.8(NM_001126105.2):c.625+1G>C (SLC7A7))
| Chromosome |
14 |
| Allele |
Paternal (confirmed) |
| 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.23249134C>G |
| DNA change (hg38) |
g.22779925C>G |
| Published as |
c.625+1G>C: p.C167_G209delinsX |
| ISCN |
- |
| DB-ID |
SLC7A7_000022 |
| Variant remarks |
1 English/Argentinean LPI family (com-het) |
| Reference |
PubMed: Font-Llitjos et al. 2009 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
yes |
| Frequency |
0/50 CON |
| 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 |
2012-12-04 16:25:21 +01:00 (CET) |
| Date last edited |
2020-07-04 15:17:16 +02:00 (CEST) |

Variant on transcripts
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