Variant #0000016953 (NC_000006.11:g.74072455G>T, NM_001017361.2:c.3G>T (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.74072455G>T |
| DNA change (hg38) |
g.73362732G>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
KHDC3L_000001 |
| Variant remarks |
Mutations found in proband and aunt of Pakistani origin with recurrent molar pregnancies (family L in Parry 2011) |
| Reference |
PubMed: Parry et al. 2011 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| Segregation |
yes |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0 View details |
| Owner |
Rosemary Fisher |
| Database submission license |
No license selected |
| Created by |
Rosemary Fisher |
| Date created |
2012-12-18 17:30:47 +01:00 (CET) |
| Date last edited |
2019-12-04 12:41:11 +01:00 (CET) |

Variant on transcripts
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