Variant #0000000032 (NC_000002.11:g.[218879593_218879600del;218879640_218879659del])
Individual ID |
00000033 |
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.[218879593_218879600del;218879640_218879659del] |
Marker/Name |
D2S1338 |
HGVS/Repeat |
g.218879582GGAA[12]GGCA[4] |
Repeat |
GGAA[12]GGCA[4] |
Published_as |
CE16-GGAA[12]GGCA[4] |
Haplotype |
D2S1338-16[A-0-0-12-4] |
dbSNP ID |
- |
Reference |
vd Gaag, in press |
DB-ID |
chr2_000004 |
Variant remarks |
- |
Genetic origin |
Germline |
Frequency |
13/198 chromosomes |
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 |
2016-06-27 12:59:20 +02:00 (CEST) |
Date last edited |
2016-06-27 22:08:56 +02:00 (CEST) |
Variant on transcripts
 |
No entries in the database yet! |
Screenings
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