Variant #0000004338 (NC_000011.9:g.68701322C>T, IGHMBP2(NM_002180.2):c.1478C>T)
Individual ID |
00004338 |
Chromosome |
11 |
Allele |
Unknown |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.68701322C>T |
Reference |
Guenther UP1, Handoko L, Varon R, Stephani U, Tsao CY, Mendell JR, Lützkendorf S, Hübner C, von Au K, Jablonka S, Dittmar G, Heinemann U, Schuetz A, Schuelke M.(2009) |
DB-ID |
IGHMBP2_000018 |
Frequency |
- |
Average frequency (gnomAD v.2.1.1) |
6.0E-5 View details |
Owner |
Y Yang |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Y Yang |

Variant on transcripts
Screenings
|
|