HNRNPM
This page contains an overview of the genetic variation in the HNRNPM gene, including its role in inherited cardiac disease. For more details, click on the links below, or for a specific variant, enter the HGVS variant here:
HNRNPM gene and transcript details
Gene Name
heterogeneous nuclear ribonucleoprotein M
Gene Links
Ensembl: ENSG00000099783 -
Locus Reference Genomic:
Genomic Location
Chromosome 19 : 8,509,883 - 8,553,738 (forward strand)
View in: Ensembl -
UCSC Genome Browser
| Canonical Seqs | Transcript (2190 bases) | Protein (730 aa) |
|---|---|---|
 |
ENST00000325495 | ENSP00000325376 |
 |
||
 |
NM_005968.4 | |
 |
P52272 |
Summary of HNRNPM in Cardiomyopathies
HNRNPM variants in ExAC
Details of the protein-altering HNRNPM variants (missense, loss of function truncating, inframe indels and splice site regions) found in the ExAC database are shown below. To view lists of specific variants with links to detailed population frequency data, click on the variant numbers - for all or a particular variant class.
| Total Variants | Combined frequency of rare variants | |
|---|---|---|
| All Variants | 244 | 0.00369 |
| Truncating | 2 | 0.00002 |
| Missense | 202 | 0.00315 |
| Inframe | 13 | 0.00027 |
| Splice Site | 27 | 0.00025 |