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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