UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.94974422C>A | CA595321708 | CYP2C9 | c.961+2177C>A (n.961+2177C>A) c.820-6761C>A (n.820-6761C>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.94974422C= | CA1929334708 | CYP2C9 | c.961+2177C= (n.961+2177C=) c.820-6761C= (n.820-6761C=) | |
| 10 | g.94974422C>G | CA670178328 | CYP2C9 | c.961+2177C>G (n.961+2177C>G) c.820-6761C>G (n.820-6761C>G) | dbSNP gnomAD v3 gnomAD v4 |
| 10 | g.94974426G>A | CA1929334710 | CYP2C9 | c.961+2181G>A (n.961+2181G>A) c.820-6757G>A (n.820-6757G>A) | dbSNP |
| 10 | g.94974426G= | CA1929334709 | CYP2C9 | c.961+2181G= (n.961+2181G=) c.820-6757G= (n.820-6757G=) | |
| 10 | g.94974427A= | CA1929334711 | CYP2C9 | c.961+2182A= (n.961+2182A=) c.820-6756A= (n.820-6756A=) | |
| 10 | g.94974427A>G | CA931402022 | CYP2C9 | c.961+2182A>G (n.961+2182A>G) c.820-6756A>G (n.820-6756A>G) | dbSNP |
| 10 | g.94974428T>A | CA1929334714 | CYP2C9 | c.961+2183T>A (n.961+2183T>A) c.820-6755T>A (n.820-6755T>A) | dbSNP |
| 10 | g.94974428T>C | CA211724606 | CYP2C9 | c.961+2183T>C (n.961+2183T>C) c.820-6755T>C (n.820-6755T>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.94974428T= | CA1929334712 | CYP2C9 | c.961+2183T= (n.961+2183T=) c.820-6755T= (n.820-6755T=) | |
| 10 | g.94974430A= | CA1929334715 | CYP2C9 | c.961+2185A= (n.961+2185A=) c.820-6753A= (n.820-6753A=) | |
| 10 | g.94974430A>G | CA1929334716 | CYP2C9 | c.961+2185A>G (n.961+2185A>G) c.820-6753A>G (n.820-6753A>G) | dbSNP |
| 10 | g.94974431T= | CA1929334717 | CYP2C9 | c.961+2186T= (n.961+2186T=) c.820-6752T= (n.820-6752T=) | |
| 10 | g.94974431_94974432insGGTAA | CA1929334719 | CYP2C9 | c.961+2186_961+2187insGGTAA (n.961+2186_961+2187insGGTAA) c.820-6752_820-6751insGGTAA (n.820-6752_820-6751insGGTAA) | dbSNP |
| 10 | g.94974432T>C | CA1929334720 | CYP2C9 | c.961+2187T>C (n.961+2187T>C) c.820-6751T>C (n.820-6751T>C) | dbSNP |
| 10 | g.94974432T= | CA1929334718 | CYP2C9 | c.961+2187T= (n.961+2187T=) c.820-6751T= (n.820-6751T=) | |
| 10 | g.94974434G>C | CA931402028 | CYP2C9 | c.961+2189G>C (n.961+2189G>C) c.820-6749G>C (n.820-6749G>C) | dbSNP gnomAD v3 gnomAD v4 |
| 10 | g.94974434G= | CA1929334721 | CYP2C9 | c.961+2189G= (n.961+2189G=) c.820-6749G= (n.820-6749G=) | |
| 10 | g.94974437A= | CA1929334724 | CYP2C9 | c.961+2192A= (n.961+2192A=) c.820-6746A= (n.820-6746A=) | |
| 10 | g.94974437A>C | CA931402030 | CYP2C9 | c.961+2192A>C (n.961+2192A>C) c.820-6746A>C (n.820-6746A>C) | dbSNP gnomAD v3 gnomAD v4 |
| 10 | g.94974437A>G | CA1929334725 | CYP2C9 | c.961+2192A>G (n.961+2192A>G) c.820-6746A>G (n.820-6746A>G) | dbSNP |
| 10 | g.94974440T>A | CA2722385682 | CYP2C9 | c.961+2195T>A (n.961+2195T>A) c.820-6743T>A (n.820-6743T>A) | dbSNP |
| 10 | g.94974440T>G | CA1929334728 | CYP2C9 | c.961+2195T>G (n.961+2195T>G) c.820-6743T>G (n.820-6743T>G) | dbSNP |
| 10 | g.94974440T= | CA1929334727 | CYP2C9 | c.961+2195T= (n.961+2195T=) c.820-6743T= (n.820-6743T=) | |
| 10 | g.94974441T>G | CA1929334730 | CYP2C9 | c.961+2196T>G (n.961+2196T>G) c.820-6742T>G (n.820-6742T>G) | dbSNP |
| 10 | g.94974441T= | CA1929334729 | CYP2C9 | c.961+2196T= (n.961+2196T=) c.820-6742T= (n.820-6742T=) | |
| 10 | g.94974442G>A | CA211724614 | CYP2C9 | c.961+2197G>A (n.961+2197G>A) c.820-6741G>A (n.820-6741G>A) | dbSNP gnomAD v3 gnomAD v4 |
| 10 | g.94974442G>C | CA1929334733 | CYP2C9 | c.961+2197G>C (n.961+2197G>C) c.820-6741G>C (n.820-6741G>C) | dbSNP |
| 10 | g.94974442G= | CA1929334732 | CYP2C9 | c.961+2197G= (n.961+2197G=) c.820-6741G= (n.820-6741G=) | |
| 10 | g.94974442G>T | CA211724619 | CYP2C9 | c.961+2197G>T (n.961+2197G>T) c.820-6741G>T (n.820-6741G>T) | dbSNP gnomAD v3 gnomAD v4 |
| 10 | g.94974443A= | CA1929334735 | CYP2C9 | c.961+2198A= (n.961+2198A=) c.820-6740A= (n.820-6740A=) | |
| 10 | g.94974443A>G | CA1929334736 | CYP2C9 | c.961+2198A>G (n.961+2198A>G) c.820-6740A>G (n.820-6740A>G) | dbSNP |
| 10 | g.94974446A= | CA1929334737 | CYP2C9 | c.961+2201A= (n.961+2201A=) c.820-6737A= (n.820-6737A=) | |
| 10 | g.94974447T>C | CA1929334741 | CYP2C9 | c.961+2202T>C (n.961+2202T>C) c.820-6736T>C (n.820-6736T>C) | dbSNP |
| 10 | g.94974447T= | CA1929334740 | CYP2C9 | c.961+2202T= (n.961+2202T=) c.820-6736T= (n.820-6736T=) | |
| 10 | g.94974452dup | CA670178333 | CYP2C9 | c.961+2207dup (n.961+2207dup) c.820-6731dup (n.820-6731dup) | dbSNP gnomAD v3 gnomAD v4 |
| 10 | g.94974453C= | CA1929334742 | CYP2C9 | c.961+2208C= (n.961+2208C=) c.820-6730C= (n.820-6730C=) | |
| 10 | g.94974453C>T | CA1929334743 | CYP2C9 | c.961+2208C>T (n.961+2208C>T) c.820-6730C>T (n.820-6730C>T) | dbSNP |
| 10 | g.94974454A= | CA1929334745 | CYP2C9 | c.961+2209A= (n.961+2209A=) c.820-6729A= (n.820-6729A=) | |
| 10 | g.94974454A>G | CA211724624 | CYP2C9 | c.961+2209A>G (n.961+2209A>G) c.820-6729A>G (n.820-6729A>G) | dbSNP |
| 10 | g.94974457A>T | CA931402036 | CYP2C9 | c.961+2212A>T (n.961+2212A>T) c.820-6726A>T (n.820-6726A>T) | gnomAD v3 gnomAD v4 |
| 10 | g.94974462G>T | CA2789073509 | CYP2C9 | c.961+2217G>T (n.961+2217G>T) c.820-6721G>T (n.820-6721G>T) | |
| 10 | g.94974463T>C | CA2789073510 | CYP2C9 | c.961+2218T>C (n.961+2218T>C) c.820-6720T>C (n.820-6720T>C) | |
| 10 | g.94974468T>A | CA2789073511 | CYP2C9 | c.961+2223T>A (n.961+2223T>A) c.820-6715T>A (n.820-6715T>A) | |
| 10 | g.94974471T>A | CA2789073512 | CYP2C9 | c.961+2226T>A (n.961+2226T>A) c.820-6712T>A (n.820-6712T>A) | |
| 10 | g.94974473G>A | CA2789073513 | CYP2C9 | c.961+2228G>A (n.961+2228G>A) c.820-6710G>A (n.820-6710G>A) | |
| 10 | g.94974473G= | CA1929334747 | CYP2C9 | c.961+2228G= (n.961+2228G=) c.820-6710G= (n.820-6710G=) | |
| 10 | g.94974473G>T | CA211724631 | CYP2C9 | c.961+2228G>T (n.961+2228G>T) c.820-6710G>T (n.820-6710G>T) | dbSNP |
| 10 | g.94974474T>A | CA2789073514 | CYP2C9 | c.961+2229T>A (n.961+2229T>A) c.820-6709T>A (n.820-6709T>A) | |
| 10 | g.94974475A= | CA1929334749 | CYP2C9 | c.961+2230A= (n.961+2230A=) c.820-6708A= (n.820-6708A=) |