Variant #0000521156 (NC_000004.11:g.110667485T>C, NM_000204.3:c.1322A>G (CFI))
| Chromosome |
4 |
| 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.110667485T>C |
| DNA change (hg38) |
g.109746329T>C |
| Published as |
CFI(NM_000204.3):c.1322A>G (p.K441R), CFI(NM_001318057.1):c.1346A>G (p.K449R), CFI(NM_001318057.2):c.1346A>G (p.K449R) |
| ISCN |
- |
| DB-ID |
CFI_000006 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) |
0.00389 View details |
| Owner |
VKGL-NL_Nijmegen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Nijmegen |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2022-11-01 13:01:21 +01:00 (CET) |

Variant on transcripts
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