gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.09662228 (SAS)
Genomes Max Group AF
0.09662228 (SAS)
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.157890467C>T , CM000668.2:g.157890467C>T | GRCh38 |
| NC_000006.11:g.158311499C>T , CM000668.1:g.158311499C>T | GRCh37 |
| NC_000006.10:g.158231487C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000392185.8:c.301-6360C>T (SNX9) MANE Select | ENSP00000376024.3:n.301-6360C>T | |
| ENST00000679691.1:c.280-6360C>T (SNX9) | ENSP00000505486.1:n.280-6360C>T | |
| ENST00000679732.1:c.301-6360C>T (SNX9) | ENSP00000505311.1:n.301-6360C>T | |
| ENST00000679790.1:c.13-11431C>T (SNX9) | ENSP00000506493.1:n.13-11431C>T | |
| ENST00000679814.1:c.301-6360C>T (SNX9) | ENSP00000506326.1:n.301-6360C>T | |
| ENST00000680015.1:n.514-6360C>T (SNX9) | ||
| ENST00000680078.1:c.301-6360C>T (SNX9) | ENSP00000505598.1:n.301-6360C>T | |
| ENST00000680089.1:n.514-6360C>T (SNX9) | ||
| ENST00000680095.1:n.514-6360C>T (SNX9) | ||
| ENST00000680464.1:n.515-6360C>T (SNX9) | ||
| ENST00000680495.1:c.-26-31064C>T (SNX9) | ENSP00000505186.1:n.-26-31064C>T | |
| ENST00000680863.1:c.390+1807C>T (SNX9) | ENSP00000505291.1:n.390+1807C>T | |
| ENST00000680974.1:n.514-6360C>T (SNX9) | ||
| ENST00000681138.1:c.13-6360C>T (SNX9) | ENSP00000505392.1:n.13-6360C>T | |
| ENST00000681183.1:c.301-6360C>T (SNX9) | ENSP00000505072.1:n.301-6360C>T | |
| ENST00000681186.1:c.301-6360C>T (SNX9) | ENSP00000506632.1:n.301-6360C>T | |
| ENST00000681534.1:c.301-6360C>T (SNX9) | ENSP00000505127.1:n.301-6360C>T | |
| ENST00000681651.1:c.*242-6360C>T (SNX9) | ENSP00000505173.1:n.*242-6360C>T | |
| ENST00000392185.7:c.301-6360C>T (SNX9) | ENSP00000376024.3:n.301-6360C>T | |
| ENST00000611124.1:c.298-6360C>T (SNX9) | ENSP00000482087.1:n.298-6360C>T | |
| NM_016224.4:c.301-6360C>T (SNX9) | NP_057308.1:n.301-6360C>T | |
| XM_005267015.1:c.280-6360C>T (SNX9) | XP_005267072.1:n.280-6360C>T | |
| XR_943168.1:n.440+2226G>A (SNX9-AS1) | ||
| XM_005267015.2:c.280-6360C>T (SNX9) | XP_005267072.1:n.280-6360C>T | |
| XR_943168.2:n.459+2226G>A (SNX9-AS1) | ||
| NM_016224.5:c.301-6360C>T (SNX9) MANE Select | NP_057308.1:n.301-6360C>T |