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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