Variant #0001032169 (NC_000001.10:g.74808631C>T, NM_015978.2:c.788C>T (TNNI3K))
| 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.74808631C>T |
| DNA change (hg38) |
- |
| Published as |
FPGT-TNNI3K(NM_001112808.2):c.1130C>T (p.P377L), FPGT-TNNI3K(NM_001112808.3):c.1091C>T (p.P364L), TNNI3K(NM_015978.2):c.788C>T (p.P263L), TNNI3K(N...) |
| ISCN |
- |
| DB-ID |
FPGT-TNNI3K_000018 See all 4 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) |
0.00244 View details |
| Owner |
VKGL-NL_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2025-05-05 21:14:00 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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