Variant #0001014378 (NC_000007.13:g.69900780dup, NC_000007.13(NM_015570.2):c.690+13dup (AUTS2))
| Chromosome |
7 |
| 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.69900780dup |
| DNA change (hg38) |
- |
| Published as |
AUTS2(NM_001127231.1):c.690+6_690+7insC (p.(=)), AUTS2(NM_015570.4):c.690+13dupC |
| ISCN |
- |
| DB-ID |
AUTS2_000069 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) |
Retrieve |
| Owner |
VKGL-NL_Groningen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Groningen |
| Date created |
2024-10-29 21:08:56 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
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