Variant #0000318038 (NC_000002.11:g.47168856C>G, NM_020458.2:c.176C>G (TTC7A))
| Chromosome |
2 |
| 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.47168856C>G |
| DNA change (hg38) |
g.46941717C>G |
| Published as |
TTC7A(NM_001288951.1):c.176C>G (p.P59R), TTC7A(NM_020458.2):c.176C>G (p.(Pro59Arg)), TTC7A(NM_020458.4):c.176C>G (p.P59R) |
| ISCN |
- |
| DB-ID |
TTC7A_000004 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) |
0.00349 View details |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2022-11-01 13:01:21 +01:00 (CET) |

Variant on transcripts
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