Variant #0000016708 (NC_000014.8:g.23245147T>C, NC_000014.8(NM_001126105.2):c.895-2A>G (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.23245147T>C |
| DNA change (hg38) |
g.22775938T>C |
| Published as |
A-to-G transition in a splice acceptor sequence 6 (IVS6-2A G) |
| ISCN |
- |
| DB-ID |
SLC7A7_000031 |
| Variant remarks |
1 Lithuanian LPI patient (hom) |
| Reference |
PubMed: Cimbalistiene et al. 2007 |
| 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 |
2012-12-04 16:25:21 +01:00 (CET) |
| Date last edited |
2020-07-04 15:16:59 +02:00 (CEST) |

Variant on transcripts
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