Variant #0000658742 (NC_000020.10:g.31620843G>T, NM_174897.2:c.151G>T (BPIFB6))
| Chromosome |
20 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.31620843G>T |
| DNA change (hg38) |
g.33033037G>T |
| Published as |
BPIFB6(NM_174897.2):c.151G>T (p.(Ala51Ser)) |
| ISCN |
- |
| DB-ID |
BPIFB6_000003 |
| 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) |
4.0E-5 View details |
| Owner |
VKGL-NL_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2020-03-23 16:13:27 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
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