Variant #0000722431 (NC_000009.11:g.140127856G>A, NM_080877.2:c.756G>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.140127856G>A |
DNA change (hg38) |
- |
Published as |
SLC34A3(NM_001177316.1):c.756G>A (p.(Gln252=)), SLC34A3(NM_001177317.1):c.756G>A (p.Q252=), SLC34A3(NM_080877.2):c.756G>A (p.Q252=) |
ISCN |
- |
DB-ID |
SLC34A3_000006 See all 3 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) |
0.00243 View details |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2021-02-08 18:36:18 +01:00 (CET) |
Date last edited |
2022-05-09 15:51:19 +02:00 (CEST) |

Variant on transcripts
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