gnomAD v2:
gnomAD v4:
Joint Max Group AF
0.00000466 (SAS)
Exomes Max Group AF
0.00000499 (SAS)
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.64622520A>C , CM000674.2:g.64622520A>C | GRCh38 |
| NC_000012.11:g.65016300A>C , CM000674.1:g.65016300A>C | GRCh37 |
| NC_000012.10:g.63302567A>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000542104.6:c.111+11777A>C (RASSF3) MANE Select | ENSP00000443021.1:n.111+11777A>C | |
| ENST00000637125.1:c.295-62267A>C (RASSF3) | ENSP00000490100.1:n.295-62267A>C | |
| ENST00000283172.8:c.111+11777A>C (RASSF3) | ENSP00000283172.4:n.111+11777A>C | |
| ENST00000336061.2:c.111+11777A>C (RASSF3) | ENSP00000336616.2:n.111+11777A>C | |
| ENST00000542104.5:c.111+11777A>C (RASSF3) | ENSP00000443021.1:n.111+11777A>C | |
| NM_178169.3:c.111+11777A>C (RASSF3) | NP_835463.1:n.111+11777A>C | |
| NR_030347.1:n.12A>C (MIR548C) | ||
| NR_037515.1:n.86T>G (MIR548Z) | ||
| NR_040718.1:n.231+11777A>C (RASSF3) | ||
| XM_011538195.1:c.75+11599A>C (RASSF3) | XP_011536497.1:n.75+11599A>C | |
| XM_011538195.2:c.75+11599A>C (RASSF3) | XP_011536497.1:n.75+11599A>C | |
| NM_178169.4:c.111+11777A>C (RASSF3) MANE Select | NP_835463.1:n.111+11777A>C | |
| NR_040718.2:n.249+11777A>C (RASSF3) |