Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.41136802A>C | CA412762566 | USP9X | c.436-2A>C (n.436-2A>C) | |
X | g.41136802A>G | CA412762568 | USP9X | c.436-2A>G (n.436-2A>G) | |
X | g.41136802A>T | CA412762571 | USP9X | c.436-2A>T (n.436-2A>T) | |
X | g.41136803G>A | CA412762580 | USP9X | c.436-1G>A (n.436-1G>A) | COSMIC |
X | g.41136803G>C | CA412762577 | USP9X | c.436-1G>C (n.436-1G>C) | |
X | g.41136803G>T | CA412762574 | USP9X | c.436-1G>T (n.436-1G>T) | |
X | g.41136804A= | CA2425806582 | USP9X | c.436A= (p.Arg146=) | |
X | g.41136804A>C | CA515966255 | USP9X | c.436A>C (p.Arg146=) | |
X | g.41136804A>G | CA10388314 | USP9X | c.436A>G (p.Arg146Gly) | dbSNP ExAC gnomAD v2 gnomAD v4 |
X | g.41136804A>T | CA412762585 | USP9X | c.436A>T (p.Arg146Trp) | |
X | g.41136805G>A | CA10388315 | USP9X | c.437G>A (p.Arg146Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.41136805G>C | CA412762590 | USP9X | c.437G>C (p.Arg146Thr) | |
X | g.41136805G= | CA2425806583 | USP9X | c.437G= (p.Arg146=) | |
X | g.41136805G>T | CA412762593 | USP9X | c.437G>T (p.Arg146Met) | |
X | g.41136806G>A | CA10388316 | USP9X | c.438G>A (p.Arg146=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.41136806G>C | CA412762598 | USP9X | c.438G>C (p.Arg146Ser) | |
X | g.41136806G= | CA2425806584 | USP9X | c.438G= (p.Arg146=) | |
X | g.41136806G>T | CA412762601 | USP9X | c.438G>T (p.Arg146Ser) | |
X | g.41136807T>A | CA412762604 | USP9X | c.439T>A (p.Cys147Ser) | |
X | g.41136807T>C | CA412762607 | USP9X | c.439T>C (p.Cys147Arg) | |
X | g.41136807T>G | CA412762610 | USP9X | c.439T>G (p.Cys147Gly) | |
X | g.41136808G>A | CA412762613 | USP9X | c.440G>A (p.Cys147Tyr) | gnomAD v4 |
X | g.41136808G>C | CA412762615 | USP9X | c.440G>C (p.Cys147Ser) | |
X | g.41136808G>T | CA412762618 | USP9X | c.440G>T (p.Cys147Phe) | |
X | g.41136809T>A | CA412762623 | USP9X | c.441T>A (p.Cys147Ter) | |
X | g.41136809T>C | CA515966262 | USP9X | c.441T>C (p.Cys147=) | dbSNP gnomAD v4 |
X | g.41136809T>G | CA412762625 | USP9X | c.441T>G (p.Cys147Trp) | |
X | g.41136809T= | CA2425806585 | USP9X | c.441T= (p.Cys147=) | |
X | g.41136810A>C | CA412762629 | USP9X | c.442A>C (p.Ile148Leu) | |
X | g.41136810A>G | CA412762632 | USP9X | c.442A>G (p.Ile148Val) | gnomAD v4 |
X | g.41136810A>T | CA412762633 | USP9X | c.442A>T (p.Ile148Phe) | |
X | g.41136811T>A | CA412762638 | USP9X | c.443T>A (p.Ile148Asn) | |
X | g.41136811T>C | CA412762639 | USP9X | c.443T>C (p.Ile148Thr) | |
X | g.41136811T>G | CA412762641 | USP9X | c.443T>G (p.Ile148Ser) | |
X | g.41136812T>A | CA515966267 | USP9X | c.444T>A (p.Ile148=) | gnomAD v4 |
X | g.41136812T>C | CA515966268 | USP9X | c.444T>C (p.Ile148=) | |
X | g.41136812T>G | CA412762644 | USP9X | c.444T>G (p.Ile148Met) | |
X | g.41136813A>C | CA412762646 | USP9X | c.445A>C (p.Ile149Leu) | |
X | g.41136813A>G | CA412762647 | USP9X | c.445A>G (p.Ile149Val) | |
X | g.41136813A>T | CA412762650 | USP9X | c.445A>T (p.Ile149Phe) | |
X | g.41136814T>A | CA412762652 | USP9X | c.446T>A (p.Ile149Asn) | |
X | g.41136814T>C | CA412762654 | USP9X | c.446T>C (p.Ile149Thr) | |
X | g.41136814T>G | CA412762656 | USP9X | c.446T>G (p.Ile149Ser) | |
X | g.41136815T>A | CA515966276 | USP9X | c.447T>A (p.Ile149=) | |
X | g.41136815T>C | CA515966279 | USP9X | c.447T>C (p.Ile149=) | |
X | g.41136815T>G | CA412762658 | USP9X | c.447T>G (p.Ile149Met) | |
X | g.41136816A= | CA2425806586 | USP9X | c.448A= (p.Asn150=) | |
X | g.41136816A>C | CA412762662 | USP9X | c.448A>C (p.Asn150His) | |
X | g.41136816A>G | CA412762660 | USP9X | c.448A>G (p.Asn150Asp) | |
X | g.41136816A>T | CA412762663 | USP9X | c.448A>T (p.Asn150Tyr) | ClinVar dbSNP gnomAD v2 gnomAD v4 |