Variant #0000550874 (NC_000013.10:g.48807583C>A, NM_021999.4:c.87C>A (ITM2B))
| Chromosome |
13 |
| 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.48807583C>A |
| DNA change (hg38) |
g.48233447C>A |
| Published as |
ITM2B(NM_021999.5):c.87C>A (p.I29=) |
| ISCN |
- |
| DB-ID |
ITM2B_000004 |
| 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_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 |
2020-07-03 16:56:15 +02:00 (CEST) |

Variant on transcripts
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