Revel Score:
ENST00000506362
0.310
gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.00021032 (SAS)
Genomes Max Group AF
0.00028182 (SAS)
Exomes Max Group AF
0.0001838 (SAS)
ClinVar Variation:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.6291939C>T , CM000666.2:g.6291939C>T | GRCh38 |
| NC_000004.11:g.6293666C>T , CM000666.1:g.6293666C>T | GRCh37 |
| NC_000004.10:g.6344567C>T | NCBI36 |
| NG_011700.1:g.27090C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682275.1:c.654C>T | ENSP00000507852.1:p.Pro218= | |
| ENST00000683395.1:c.631C>T | ||
| ENST00000684087.1:c.654C>T | ENSP00000506978.1:p.Pro218= | |
| ENST00000506362.2:c.405C>T | ENSP00000424103.2:p.Pro135= | |
| ENST00000673642.1:c.453C>T | ENSP00000501242.1:p.Pro151= | |
| ENST00000673991.1:c.654C>T | ENSP00000501033.1:p.Pro218= | |
| ENST00000226760.5:c.654C>T MANE Select | ENSP00000226760.1:p.Pro218= | |
| ENST00000503569.5:c.654C>T | ENSP00000423337.1:p.Pro218= | |
| ENST00000506362.1:c.251C>T | ||
| ENST00000507765.1:n.839C>T | ||
| NM_001145853.1:c.654C>T | NP_001139325.1:p.Pro218= | |
| NM_006005.3:c.654C>T MANE Select | NP_005996.2:p.Pro218= | |
| XM_017008586.1:c.663C>T | XP_016864075.1:p.Pro221= |