Variant #0000244026 (NC_000003.11:g.87377739C>T, NM_014043.3:c.(312C>T) (CHMP2B))
| Chromosome |
3 |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Effect unknown |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.87377739C>T |
| DNA change (hg38) |
- |
| Published as |
- |
| ISCN |
- |
| DB-ID |
CHMP2B_000011 |
| Variant remarks |
Corresponds to SNP <a href=\""http://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?rs=13100218"""" target=""""_blank"""">rs13100218</a>. /r/Silent point mutation in coding region"" Variant Error [EREF/EUNCERTAIN]: This genomic variant does not match the reference sequence; the transcript variant also has an error. Please fix this entry and then remove this message. |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs11540913 |
| Origin |
Unknown |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Marc Cruts |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
Julia Lopez |
| Date created |
2013-05-01 13:44:57 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
|