Variant #0000078723 (NC_000005.9:g.(176600001_180915260)_qterdelins[NC_000023.10:pter_(33038318_33229398)inv])
Individual ID |
00049886 |
Chromosome |
5 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
VUS |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.(176600001_180915260)_qterdelins[NC_000023.10:pter_(33038318_33229398)inv] |
DNA change (hg38) |
- |
Published as |
- |
ISCN |
t(X;5)(p21.1;q35.3) |
DB-ID |
chr5_001040 |
Variant remarks |
translocation |
Reference |
PubMed: Meitinger 1988, Journal: Meitinger 1988 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Unknown |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Genomic location of variant could not be determined |
Owner |
Johan den Dunnen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |
Date created |
2015-09-14 15:28:52 +02:00 (CEST) |
Date last edited |
2020-05-12 19:21:26 +02:00 (CEST) |
Variant on transcripts
Screenings
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