Variant #0000505114 (NC_000001.10:g.214557062_214557067del, NM_005401.4:c.2144_2149del (PTPN14))
| Chromosome |
1 |
| 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.214557062_214557067del |
| DNA change (hg38) |
g.214383719_214383724del |
| Published as |
PTPN14(NM_005401.4):c.2144_2149delAGGAGG (p.E715_E716del) |
| ISCN |
- |
| DB-ID |
PTPN14_000028 |
| 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 |
2020-03-23 16:13:27 +01:00 (CET) |

Variant on transcripts
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