Variant #0000369868 (NC_000016.9:g.1412140_1412168del, NC_000016.9(NM_032520.4):c.411+8_411+35del (GNPTG))
| Chromosome |
16 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Affects function |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.1412140_1412168del |
| DNA change (hg38) |
- |
| Published as |
- |
| ISCN |
- |
| DB-ID |
GNPTG_000076 |
| Variant remarks |
Variant Error [EMISMATCH]: This variant seems to mismatch; the genomic and the transcript variant seems to not belong together. Please fix this entry and then remove this message. |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Renata Voltolini Velho |
| Database submission license |
No license selected |
| Created by |
Renata Voltolini Velho |
| Date created |
2018-06-27 12:55:25 +02:00 (CEST) |
| Date last edited |
2018-06-27 12:58:11 +02:00 (CEST) |

Variant on transcripts
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