Variant #0000061112 (NC_000002.11:g.(28789666_28796008)_(29320823_29337003)dup)
Individual ID |
00034036 |
Chromosome |
2 |
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.(28789666_28796008)_(29320823_29337003)dup |
DNA change (hg38) |
- |
Published as |
g.(28789666_28796008)_(29320823_29337003)dup |
ISCN |
- |
DB-ID |
chr2_000387 |
Variant remarks |
- |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
De novo |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Marta Sanchez Castro |
Database submission license |
No license selected |
Created by |
Marta Sanchez Castro |
Date created |
2015-03-09 02:05:47 +01:00 (CET) |
Date last edited |
2015-03-20 11:21:00 +01:00 (CET) |

Variant on transcripts
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