Variant #0000885110 (NC_000002.11:g.27427681G>A, NM_021095.2:c.853C>T (SLC5A6))
| Chromosome |
2 |
| 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.27427681G>A |
| DNA change (hg38) |
- |
| Published as |
SLC5A6(NM_021095.4):c.853C>T (p.(Arg285Cys), p.R285C) |
| ISCN |
- |
| DB-ID |
SLC5A6_000013 See all 2 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) |
3.0E-5 View details |
| Owner |
VKGL-NL_VUmc |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_VUmc |
| Date created |
2022-11-01 13:01:21 +01:00 (CET) |
| Date last edited |
2024-04-19 20:20:39 +02:00 (CEST) |

Variant on transcripts
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