Variant #0000523514 (NC_000004.11:g.89013403_89013425dup, NM_004827.2:c.1930_1952dup (ABCG2))
| Chromosome |
4 |
| 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.89013403_89013425dup |
| DNA change (hg38) |
g.88092251_88092273dup |
| Published as |
ABCG2(NM_004827.2):c.1930_1952dupGCCTACCTGAAATTGTTATTTCT (p.K652Pfs*3) |
| ISCN |
- |
| DB-ID |
ABCG2_000002 |
| 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_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2020-06-16 13:35:10 +02:00 (CEST) |

Variant on transcripts
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