Variant #0000000005 (NC_000002.11:g.218879582_218879673=)
| Individual ID |
00000008 |
| Chromosome |
2 |
| 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.218879582_218879673= |
| Marker/Name |
D2S1338 |
| HGVS/Repeat |
g.218879582GGAA[2]GGAC[1]GGAA[13]GGCA[7] |
| Repeat |
GGAA[2]GGAC[1]GGAA[13]GGCA[7] |
| Published_as |
TGCC[7]TTCC[13]GTCC[1]TTCC[2] |
| Haplotype |
D2S1338-23 |
| dbSNP ID |
- |
| Reference |
Parson 2016, Parson 2016 |
| DB-ID |
chr2_000001 See all 2 reported entries |
| Variant remarks |
length capillary electrophoresis 23 |
| Genetic origin |
Germline |
| Frequency |
- |
| Average frequency (gnomAD v.2.1.1) |
Genomic location of variant could not be determined |
| Owner |
Jamie Zeegers |
| Database submission license |
No license selected |
| Created by |
Jamie Zeegers |
| Date created |
2016-06-27 09:36:39 +02:00 (CEST) |
| Date last edited |
N/A |
Variant on transcripts
 |
No entries in the database yet! |
Screenings
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