Variant #0000309091 (NC_000017.10:g.37821649_37821651del, NM_003673.3:c.37_39del (TCAP))
| Chromosome |
17 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.37821649_37821651del |
| DNA change (hg38) |
g.39665396_39665398del |
| Published as |
TCAP(NM_003673.3):c.37_39del (p.(Glu13del)), TCAP(NM_003673.3):c.37_39delGAG (p.E13del), TCAP(NM_003673.4):c.37_39delGAG (p.E13del) |
| ISCN |
- |
| DB-ID |
TCAP_000010 See all 18 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_AMC |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_AMC |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2023-04-16 21:50:28 +02:00 (CEST) |

Variant on transcripts
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