Variant #0000816547 (NC_000007.13:g.69064692C>A, NM_015570.2:c.53C>A (AUTS2))
| Chromosome |
7 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Probably affects function |
| Classification method |
ACMG |
| Clinical classification |
likely pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.69064692C>A |
| DNA change (hg38) |
g.69599706C>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
AUTS2_000117 |
| Variant remarks |
Heterozygous variant was observed in the product of conception after a spontaneous abortion at gestational week 8 and 3/7 |
| Reference |
PubMed: Zhao et al., 2021 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline/De novo (untested) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Alexander Groffen |
| Database submission license |
Creative Commons Attribution-ShareAlike 4.0 International |
| Created by |
Alexander Groffen |
| Date created |
2021-10-26 15:02:40 +02:00 (CEST) |
| Date last edited |
2021-10-27 09:17:39 +02:00 (CEST) |

Variant on transcripts
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