Variant #0000915491 (NC_000022.10:g.23653976_23653979dup, NM_004327.3:c.3275_3278dup (BCR))
Chromosome |
22 |
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.23653976_23653979dup |
DNA change (hg38) |
- |
Published as |
BCR(NM_004327.3):c.3274_3275insCCGG (p.(Val1094ArgfsTer17)), BCR(NM_004327.3):c.3275_3278dupCCGG (p.V1094Rfs*17), BCR(NM_004327.4):c.3275_3278dupCC... |
ISCN |
- |
DB-ID |
BCR_000014 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) |
Retrieve |
Owner |
VKGL-NL_Groningen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Groningen |
Date created |
2023-01-11 15:44:22 +01:00 (CET) |
Date last edited |
N/A |

Variant on transcripts
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