Variant #0000001417 (NC_000006.11:g.74072970_74072973del, NM_001017361.2:c.322_325del (KHDC3L))
| Chromosome |
6 |
| Allele |
Both (homozygous) |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Effect unknown |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.74072970_74072973del |
| DNA change (hg38) |
g.73363247_73363250del |
| Published as |
- |
| ISCN |
- |
| DB-ID |
KHDC3L_000002 |
| Variant remarks |
Mutation found in individual of Tunisian origin with recurrent molar pregnancies (family T in Parry 2011) |
| Reference |
PubMed: Parry et al. 2011 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| Segregation |
? |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Rosemary Fisher |
| Database submission license |
No license selected |
| Created by |
Rosemary Fisher |
| Date created |
2012-07-17 13:57:58 +02:00 (CEST) |
| Date last edited |
2020-06-19 14:59:46 +02:00 (CEST) |

Variant on transcripts
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