gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.00008238 (AFR)
Genomes Max Group AF
0.00003293 (AFR)
Exomes Max Group AF
0.00009753 (AFR)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.147657804G>A , CM000666.2:g.147657804G>A | GRCh38 |
| NC_000004.11:g.148578955G>A , CM000666.1:g.148578955G>A | GRCh37 |
| NC_000004.10:g.148798405G>A | NCBI36 |
| NG_053105.1:g.31427C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000322396.7:c.1318C>T (PRMT9) MANE Select | ENSP00000314396.6:p.Gln440Ter | |
| ENST00000322396.6:c.1318C>T (PRMT9) | ENSP00000314396.6:p.Gln440Ter | |
| ENST00000508208.5:c.780-14063G>A (TMEM184C) | ENSP00000425940.1:n.780-14063G>A | |
| ENST00000510269.5:n.645C>T (PRMT9) | ||
| ENST00000514886.1:c.*968C>T (PRMT9) | ENSP00000426732.1:n.*968C>T | |
| NM_001304458.1:c.979C>T (PRMT9) | NP_001291387.1:p.Gln327Ter | |
| NM_138364.3:c.1318C>T (PRMT9) | NP_612373.2:p.Gln440Ter | |
| XM_005263338.1:c.1081C>T (PRMT9) | XP_005263395.1:p.Gln361Ter | |
| XM_005263340.2:c.403C>T (PRMT9) | XP_005263397.1:p.Gln135Ter | |
| NM_001350141.1:c.250C>T (PRMT9) | NP_001337070.1:p.Gln84Ter | |
| NM_001350142.1:c.979C>T (PRMT9) | NP_001337071.1:p.Gln327Ter | |
| NM_001350143.1:c.403C>T (PRMT9) | NP_001337072.1:p.Gln135Ter | |
| NM_001350144.1:c.94C>T (PRMT9) | NP_001337073.1:p.Gln32Ter | |
| XM_017008823.2:c.403C>T (PRMT9) | XP_016864312.1:p.Gln135Ter | |
| XM_017008824.2:c.403C>T (PRMT9) | XP_016864313.1:p.Gln135Ter | |
| XM_017008825.1:c.403C>T (PRMT9) | XP_016864314.1:p.Gln135Ter | |
| XM_017008826.1:c.403C>T (PRMT9) | XP_016864315.1:p.Gln135Ter | |
| NM_138364.4:c.1318C>T (PRMT9) MANE Select | NP_612373.2:p.Gln440Ter | |
| NM_001304458.2:c.979C>T (PRMT9) | NP_001291387.1:p.Gln327Ter | |
| NM_001350141.2:c.250C>T (PRMT9) | NP_001337070.1:p.Gln84Ter | |
| NM_001350142.2:c.979C>T (PRMT9) | NP_001337071.1:p.Gln327Ter | |
| NM_001350143.2:c.403C>T (PRMT9) | NP_001337072.1:p.Gln135Ter | |
| NM_001350144.2:c.94C>T (PRMT9) | NP_001337073.1:p.Gln32Ter |