Variant #0000665705 (NC_000008.10:g.[NC_000019.9:(35762292_35940346)_qter]delins(119038109_119106577)_qter)
Individual ID |
00133225 |
Chromosome |
8 |
Allele |
Unknown |
Affects function (as reported) |
Probably affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.[NC_000019.9:(35762292_35940346)_qter]delins(119038109_119106577)_qter |
DNA change (hg38) |
- |
Published as |
- |
ISCN |
t(8;19)(q24.11;q13.13) |
DB-ID |
chr8_000000 See all 5 reported entries |
Variant remarks |
BAC clones RP11-89P19, RP11-260I14, and RP11-2D13 give split signal |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
DUPLICATE record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Genomic location of variant could not be determined |
Owner |
Ivy Jennes |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Johan den Dunnen |
Date created |
2020-05-13 12:08:02 +02:00 (CEST) |
Date last edited |
N/A |
Variant on transcripts
Screenings
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