Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.41136792del | CA2693506265 | USP9X | c.436-12del (n.436-12del) | gnomAD v4 |
X | g.41136790C>A | CA2425806575 | USP9X | c.436-14C>A (n.436-14C>A) | dbSNP |
X | g.41136790C= | CA2425806574 | USP9X | c.436-14C= (n.436-14C=) | |
X | g.41136790C>G | CA875381323 | USP9X | c.436-14C>G (n.436-14C>G) | dbSNP gnomAD v3 gnomAD v4 |
X | g.41136790C>T | CA641899618 | USP9X | c.436-14C>T (n.436-14C>T) | dbSNP gnomAD v2 gnomAD v4 |
X | g.41136791C>A | CA2693506269 | USP9X | c.436-13C>A (n.436-13C>A) | dbSNP gnomAD v4 |
X | g.41136791C= | CA2425806576 | USP9X | c.436-13C= (n.436-13C=) | |
X | g.41136791C>G | CA2425806577 | USP9X | c.436-13C>G (n.436-13C>G) | dbSNP |
X | g.41136792C>A | CA641899619 | USP9X | c.436-12C>A (n.436-12C>A) | dbSNP gnomAD v2 gnomAD v4 |
X | g.41136792C= | CA2425806578 | USP9X | c.436-12C= (n.436-12C=) | |
X | g.41136792C>T | CA641899620 | USP9X | c.436-12C>T (n.436-12C>T) | dbSNP gnomAD v2 gnomAD v4 |
X | g.41136793T>C | CA2693506270 | USP9X | c.436-11T>C (n.436-11T>C) | gnomAD v4 |
X | g.41136793T>G | CA2579587365 | USP9X | c.436-11T>G (n.436-11T>G) | |
X | g.41136795G>A | CA2693506271 | USP9X | c.436-9G>A (n.436-9G>A) | gnomAD v4 |
X | g.41136795G= | CA2425806579 | USP9X | c.436-9G= (n.436-9G=) | |
X | g.41136795G>T | CA1132559659 | USP9X | c.436-9G>T (n.436-9G>T) | dbSNP gnomAD v3 gnomAD v4 |
X | g.41136797A= | CA2425806580 | USP9X | c.436-7A= (n.436-7A=) | |
X | g.41136797A>C | CA2693506272 | USP9X | c.436-7A>C (n.436-7A>C) | dbSNP gnomAD v4 |
X | g.41136797A>G | CA10388313 | USP9X | c.436-7A>G (n.436-7A>G) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.41136800A= | CA2425806581 | USP9X | c.436-4A= (n.436-4A=) | |
X | g.41136800A>G | CA2693506273 | USP9X | c.436-4A>G (n.436-4A>G) | gnomAD v4 |
X | g.41136800A>T | CA1132559662 | USP9X | c.436-4A>T (n.436-4A>T) | dbSNP gnomAD v3 gnomAD v4 |
X | g.41136801C>A | CA2693506274 | USP9X | c.436-3C>A (n.436-3C>A) | gnomAD v4 |
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) |