Variant #0000050412 (NC_000014.8:g.101179660_101179695TG[9])
| Individual ID |
00027198 |
| Chromosome |
14 |
| Allele |
Maternal (confirmed) |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.101179660_101179695TG[9] |
| DNA change (hg38) |
- |
| Published as |
D14S1006:126 |
| ISCN |
- |
| DB-ID |
chr14_000129 |
| Variant remarks |
haplotype analysis shows biparental inheritance (D14S80-98, D14S608-197, D14S588-130, D14S1000-126, D14S617-143, D14S985-129, D14S1010-144, D14S292-108) |
| Reference |
PubMed: Kagami 2014 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2014-12-29 17:00:06 +01:00 (CET) |
| Date last edited |
2019-08-17 12:37:01 +02:00 (CEST) |

Variant on transcripts
Screenings
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