Variant #0000332952 (NC_000009.11:g.140127809G>A, NM_080877.2:c.709G>A (SLC34A3))
| Chromosome |
9 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.140127809G>A |
| DNA change (hg38) |
g.137233357G>A |
| Published as |
SLC34A3(NM_001177316.1):c.709G>A (p.(Asp237Asn)), SLC34A3(NM_001177317.1):c.709G>A (p.D237N), SLC34A3(NM_080877.2):c.709G>A (p.D237N) |
| ISCN |
- |
| DB-ID |
SLC34A3_000005 See all 4 reported entries |
| Variant remarks |
VKGL data sharing initiative Nederland |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
CLASSIFICATION record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00161 View details |
| Owner |
VKGL-NL_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2022-11-01 13:01:21 +01:00 (CET) |

Variant on transcripts
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