Variant #0000531755 (NC_000007.13:g.26237238A>G, NC_000007.13(NM_002137.3):c.117+4T>C (HNRNPA2B1))
| Chromosome |
7 |
| 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.26237238A>G |
| DNA change (hg38) |
g.26197618A>G |
| Published as |
HNRNPA2B1(NM_002137.4):c.117+4T>C, HNRNPA2B1(NM_031243.2):c.153+4T>C, HNRNPA2B1(NM_031243.3):c.153+4T>C |
| ISCN |
- |
| DB-ID |
CBX3_000004 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) |
0.02875 View details |
| 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 |
2025-05-05 21:14:00 +02:00 (CEST) |

Variant on transcripts
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