Variant #0000000004 (NC_000001.10:g.230905352_230905429=)
| Individual ID |
00000007 |
| Chromosome |
1 |
| Allele |
Parent #1 |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Does not affect function |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.230905352_230905429= |
| Marker/Name |
D1S1656 |
| HGVS/Repeat |
g.230905352CA[5]CCTA[1]TCTC[16] |
| Repeat |
CA[5]CCTA[1]TCTC[16] |
| Published_as |
[TAGA]16TAGG[TG]5 |
| Haplotype |
D1S1656-17 |
| dbSNP ID |
- |
| Reference |
Parson 2016, Parson 2016 |
| DB-ID |
chr1_000001 |
| Variant remarks |
length capillary electrophoresis 17 |
| Genetic origin |
Germline |
| Frequency |
- |
| Average frequency (gnomAD v.2.1.1) |
Genomic location of variant could not be determined |
| Owner |
Johan den Dunnen |
| Database submission license |
No license selected |
| Created by |
Johan den Dunnen |
| Date created |
2016-06-20 09:16:54 +02:00 (CEST) |
| Date last edited |
2016-06-27 11:04:13 +02:00 (CEST) |
Variant on transcripts
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No entries in the database yet! |
Screenings
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