Variant #0000542704 (NC_000011.9:g.119216832G>A, NM_031433.2:c.195C>T (MFRP))
| Chromosome |
11 |
| 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.119216832G>A |
| DNA change (hg38) |
g.119346122G>A |
| Published as |
C1QTNF5(NM_015645.5):c.-2442C>T, MFRP(NM_031433.3):c.195C>T (p.F65=), MFRP(NM_031433.4):c.195C>T (p.F65=) |
| ISCN |
- |
| DB-ID |
C1QTNF5_000023 See all 2 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) |
0.00128 View details |
| 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 |
2024-02-26 20:06:56 +01:00 (CET) |

Variant on transcripts
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