Variant #0000619777 (NC_000023.10:g.66765219_66765227dup, NM_000044.3:c.231_239dup (AR))
| Chromosome |
X |
| 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.66765219_66765227dup |
| DNA change (hg38) |
g.67545377_67545385dup |
| Published as |
AR(NM_000044.3):c.171_179dup (p.(Gln60_Gln61insGlnGlnGln)), AR(NM_000044.4):c.231_239dupGCAGCAGCA (p.Q78_Q80dup), AR(NM_000044.6):c.231_239dupGCAGC... |
| ISCN |
- |
| DB-ID |
AR_000622 See all 12 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) |
Retrieve |
| Owner |
VKGL-NL_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2019-12-04 15:24:38 +01:00 (CET) |
| Date last edited |
2024-02-26 20:06:56 +01:00 (CET) |

Variant on transcripts
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