Variant #0000154151 (NC_000005.9:g.176813493G>C, NM_003052.4:c.458G>C (SLC34A1))
| Chromosome |
5 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.176813493G>C |
| DNA change (hg38) |
g.177386492G>C |
| Published as |
- |
| ISCN |
- |
| DB-ID |
SLC34A1_000005 See all 4 reported entries |
| Variant remarks |
cDNA expression cloning in Xenopus oocytes showed no induced P-uptake/in Opossum kidney cells showed complete intra-cellular retention and no actin co-localisation |
| Reference |
PubMed: Schlingmann 2016, Journal: Schlingmann 2016 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0 View details |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2017-01-07 11:59:01 +01:00 (CET) |
| Date last edited |
2025-03-03 12:01:36 +01:00 (CET) |

Variant on transcripts
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