Variant #0000613909 (NC_000012.11:g.121175678C>T, NM_000017.2:c.511C>T (ACADS))
| Chromosome |
12 |
| 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.121175678C>T |
| DNA change (hg38) |
g.120737875C>T |
| Published as |
ACADS(NM_000017.2):c.511C>T (p.(Arg171Trp)), ACADS(NM_000017.3):c.511C>T (p.R171W), ACADS(NM_000017.4):c.511C>T (p.R171W) |
| ISCN |
- |
| DB-ID |
ACADS_000009 See all 5 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) |
0.03117 View details |
| Owner |
VKGL-NL_Nijmegen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Nijmegen |
| Date created |
2019-12-04 15:24:38 +01:00 (CET) |
| Date last edited |
2024-08-28 13:16:32 +02:00 (CEST) |

Variant on transcripts
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