Variant #0000016698 (NC_000014.8:g.23249134C>T, NC_000014.8(NM_001126105.2):c.625+1G>A (SLC7A7))
| Chromosome |
14 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Affects function |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.23249134C>T |
| DNA change (hg38) |
g.22779925C>T |
| Published as |
911+1G>A; IVS4+1G>A |
| ISCN |
- |
| DB-ID |
SLC7A7_000021 |
| Variant remarks |
1 Turkish (hom) and 1 Korean (hom) LPI family, 3 Japanese (com-het) LPI families; Mutation causes exon 4 skipping |
| Reference |
PubMed: Mykkanen et al. 2000, PubMed: Noguchi et al.v2000, PubMed: Ko et al. 2012 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
yes |
| Frequency |
0/50 JAP CON |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
4.0E-5 View details |
| 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 |
2017-05-05 19:04:32 +02:00 (CEST) |

Variant on transcripts
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