Variant #0000544777 (NC_000011.9:g.62457948A>G, NM_001122955.3:c.1280T>C (BSCL2))
| 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.62457948A>G |
| DNA change (hg38) |
g.62690476A>G |
| Published as |
BSCL2(NM_001122955.3):c.1280T>C (p.L427P, p.(Leu427Pro)), BSCL2(NM_001122955.4):c.1280T>C (p.L427P), BSCL2(NM_032667.6):c.1088T>C (p.L363P) |
| ISCN |
- |
| DB-ID |
BSCL2_000030 See all 8 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) |
0.00352 View details |
| Owner |
VKGL-NL_AMC |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_AMC |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2023-01-11 15:44:22 +01:00 (CET) |

Variant on transcripts
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