Variant #0000621979 (NC_000008.10:g.11405576G>A, NM_001715.2:c.211G>A (BLK))
| Chromosome |
8 |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.11405576G>A |
| DNA change (hg38) |
g.11548067G>A |
| Published as |
BLK(NM_001330465.1):c.-3G>A (p.(=)), BLK(NM_001715.3):c.211G>A (p.A71T) |
| ISCN |
- |
| DB-ID |
BLK_000003 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) |
0.01157 View details |
| Owner |
VKGL-NL_Utrecht |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Utrecht |
| Date created |
2019-12-06 12:43:26 +01:00 (CET) |
| Date last edited |
2023-04-16 21:50:28 +02:00 (CEST) |

Variant on transcripts
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