Variant #0000017180 (NC_000006.11:g.74072947_74072950del, NM_001017361.2:c.299_302del (KHDC3L))
| Chromosome |
6 |
| Allele |
Both (homozygous) |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Affects function |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.74072947_74072950del |
| DNA change (hg38) |
g.73363224_73363227del |
| Published as |
- |
| ISCN |
- |
| DB-ID |
KHDC3L_000004 |
| Variant remarks |
Mutation found in individual of African-American origin with recurrent molar pregnancies (MoUS70 in Reddy 2013) |
| Reference |
PubMed: Reddy et al. 2013 |
| 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 |
2013-03-14 10:16:36 +01:00 (CET) |
| Date last edited |
2020-06-19 14:59:46 +02:00 (CEST) |

Variant on transcripts
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