Variant #0000523391 (NC_000004.11:g.88535850_88535867dup, NM_014208.3:c.2036_2053dup (DSPP))
| Chromosome |
4 |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.88535850_88535867dup |
| DNA change (hg38) |
g.87614698_87614715dup |
| Published as |
DSPP(NM_014208.3):c.2018_2019insTAGCAGTGACAGCAGCAG (p.(Asp673_Ser674insSerSerAspSerSerSer)), DSPP(NM_014208.3):c.2036_2053dupGTAGCAGTGACAGCAGCA (p...) |
| ISCN |
- |
| DB-ID |
DSPP_000058 See all 3 reported entries |
| Variant remarks |
VKGL data sharing initiative Nederland |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
CLASSIFICATION record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2019-12-04 15:24:38 +01:00 (CET) |

Variant on transcripts
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