Variant #0000254025 (NC_000010.10:g.73121938A>G, NM_018344.5:c.1001A>G (SLC29A3))
| Chromosome |
10 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.73121938A>G |
| DNA change (hg38) |
g.71362181A>G |
| Published as |
SLC29A3(NM_001174098.1):c.*230A>G (p.(=)), SLC29A3(NM_001363518.1):c.767A>G (p.N256S), SLC29A3(NM_018344.6):c.1001A>G (p.N334S) |
| ISCN |
- |
| DB-ID |
SLC29A3_000029 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) |
0.00054 View details |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2022-05-09 15:51:19 +02:00 (CEST) |

Variant on transcripts
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