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 |
|---|---|---|---|---|---|
| 15 | g.66435014del | CA7623867 | MAP2K1 | c.15-13del (n.15-13del) c.81-13del (n.81-13del) n.517-13del n.592-13del | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.66435014C>A | CA2629081320 | MAP2K1 | c.15-13C>A (n.15-13C>A) c.81-13C>A (n.81-13C>A) n.517-13C>A n.592-13C>A | dbSNP gnomAD v4 |
| 15 | g.66435014C= | CA2184071699 | MAP2K1 | c.15-13C= (n.15-13C=) c.81-13C= (n.81-13C=) n.517-13C= n.592-13C= | |
| 15 | g.66435014C>T | CA7623868 | MAP2K1 | c.15-13C>T (n.15-13C>T) c.81-13C>T (n.81-13C>T) n.517-13C>T n.592-13C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.66435015A= | CA2184071700 | MAP2K1 | c.15-12A= (n.15-12A=) c.81-12A= (n.81-12A=) n.517-12A= n.592-12A= | |
| 15 | g.66435015A>C | CA7623869 | MAP2K1 | c.15-12A>C (n.15-12A>C) c.81-12A>C (n.81-12A>C) n.517-12A>C n.592-12A>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.66435015A>G | CA715006826 | MAP2K1 | c.15-12A>G (n.15-12A>G) c.81-12A>G (n.81-12A>G) n.517-12A>G n.592-12A>G | ClinVar dbSNP gnomAD v4 |
| 15 | g.66435015A>T | CA2730917001 | MAP2K1 | c.15-12A>T (n.15-12A>T) c.81-12A>T (n.81-12A>T) n.517-12A>T n.592-12A>T | dbSNP |
| 15 | g.66435016C>A | CA2629081321 | MAP2K1 | c.15-11C>A (n.15-11C>A) c.81-11C>A (n.81-11C>A) n.517-11C>A n.592-11C>A | gnomAD v4 |
| 15 | g.66435017T>A | CA2629081323 | MAP2K1 | c.15-10T>A (n.15-10T>A) c.81-10T>A (n.81-10T>A) n.517-10T>A n.592-10T>A | dbSNP gnomAD v4 |
| 15 | g.66435017T>C | CA2731110155 | MAP2K1 | c.15-10T>C (n.15-10T>C) c.81-10T>C (n.81-10T>C) n.517-10T>C n.592-10T>C | dbSNP |
| 15 | g.66435019del | CA2629081322 | MAP2K1 | c.15-8del (n.15-8del) c.81-8del (n.81-8del) n.517-8del n.592-8del | gnomAD v4 |
| 15 | g.66435018T>C | CA2730917392 | MAP2K1 | c.15-9T>C (n.15-9T>C) c.81-9T>C (n.81-9T>C) n.517-9T>C n.592-9T>C | dbSNP |
| 15 | g.66435018T>G | CA7623870 | MAP2K1 | c.15-9T>G (n.15-9T>G) c.81-9T>G (n.81-9T>G) n.517-9T>G n.592-9T>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.66435018T= | CA2184071701 | MAP2K1 | c.15-9T= (n.15-9T=) c.81-9T= (n.81-9T=) n.517-9T= n.592-9T= | |
| 15 | g.66435019T>C | CA2629081324 | MAP2K1 | c.15-8T>C (n.15-8T>C) c.81-8T>C (n.81-8T>C) n.517-8T>C n.592-8T>C | gnomAD v4 |
| 15 | g.66435019T>G | CA2575765955 | MAP2K1 | c.15-8T>G (n.15-8T>G) c.81-8T>G (n.81-8T>G) n.517-8T>G n.592-8T>G | |
| 15 | g.66435020G>A | CA2629081325 | MAP2K1 | c.15-7G>A (n.15-7G>A) c.81-7G>A (n.81-7G>A) n.517-7G>A n.592-7G>A | dbSNP gnomAD v4 |
| 15 | g.66435020G>C | CA2697549134 | MAP2K1 | c.15-7G>C (n.15-7G>C) c.81-7G>C (n.81-7G>C) n.517-7G>C n.592-7G>C | ClinVar dbSNP |
| 15 | g.66435020G>T | CA2731110159 | MAP2K1 | c.15-7G>T (n.15-7G>T) c.81-7G>T (n.81-7G>T) n.517-7G>T n.592-7G>T | dbSNP |
| 15 | g.66435021del | CA2731110161 | MAP2K1 | c.15-6del (n.15-6del) c.81-6del (n.81-6del) n.517-6del n.592-6del | dbSNP |
| 15 | g.66435021G>A | CA2730917393 | MAP2K1 | c.15-6G>A (n.15-6G>A) c.81-6G>A (n.81-6G>A) n.517-6G>A n.592-6G>A | dbSNP |
| 15 | g.66435021G>C | CA271640639 | MAP2K1 | c.15-6G>C (n.15-6G>C) c.81-6G>C (n.81-6G>C) n.517-6G>C n.592-6G>C | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.66435021G= | CA2184071702 | MAP2K1 | c.15-6G= (n.15-6G=) c.81-6G= (n.81-6G=) n.517-6G= n.592-6G= | |
| 15 | g.66435021G>T | CA2629081326 | MAP2K1 | c.15-6G>T (n.15-6G>T) c.81-6G>T (n.81-6G>T) n.517-6G>T n.592-6G>T | dbSNP gnomAD v4 |
| 15 | g.66435022A= | CA2184071703 | MAP2K1 | c.15-5A= (n.15-5A=) c.81-5A= (n.81-5A=) n.517-5A= n.592-5A= | |
| 15 | g.66435022A>C | CA2184071704 | MAP2K1 | c.15-5A>C (n.15-5A>C) c.81-5A>C (n.81-5A>C) n.517-5A>C n.592-5A>C | dbSNP |
| 15 | g.66435022A>G | CA2629081327 | MAP2K1 | c.15-5A>G (n.15-5A>G) c.81-5A>G (n.81-5A>G) n.517-5A>G n.592-5A>G | dbSNP gnomAD v4 |
| 15 | g.66435022A>T | CA2731033598 | MAP2K1 | c.15-5A>T (n.15-5A>T) c.81-5A>T (n.81-5A>T) n.517-5A>T n.592-5A>T | dbSNP |
| 15 | g.66435023A= | CA2184071705 | MAP2K1 | c.15-4A= (n.15-4A=) c.81-4A= (n.81-4A=) n.517-4A= n.592-4A= | |
| 15 | g.66435023A>C | CA970929822 | MAP2K1 | c.15-4A>C (n.15-4A>C) c.81-4A>C (n.81-4A>C) n.517-4A>C n.592-4A>C | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.66435023A>G | CA970929824 | MAP2K1 | c.15-4A>G (n.15-4A>G) c.81-4A>G (n.81-4A>G) n.517-4A>G n.592-4A>G | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.66435023A>T | CA2731033600 | MAP2K1 | c.15-4A>T (n.15-4A>T) c.81-4A>T (n.81-4A>T) n.517-4A>T n.592-4A>T | dbSNP |
| 15 | g.66435024C>A | CA2730916598 | MAP2K1 | c.15-3C>A (n.15-3C>A) c.81-3C>A (n.81-3C>A) n.517-3C>A n.592-3C>A | dbSNP |
| 15 | g.66435024C= | CA2184071706 | MAP2K1 | c.15-3C= (n.15-3C=) c.81-3C= (n.81-3C=) n.517-3C= n.592-3C= | |
| 15 | g.66435024C>G | CA2629081328 | MAP2K1 | c.15-3C>G (n.15-3C>G) c.81-3C>G (n.81-3C>G) n.517-3C>G n.592-3C>G | dbSNP gnomAD v4 |
| 15 | g.66435024C>T | CA7623871 | MAP2K1 | c.15-3C>T (n.15-3C>T) c.81-3C>T (n.81-3C>T) n.517-3C>T n.592-3C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.66435025A>C | CA392928850 | MAP2K1 | c.15-2A>C (n.15-2A>C) c.81-2A>C (n.81-2A>C) n.517-2A>C n.592-2A>C | dbSNP |
| 15 | g.66435025A>G | CA392928852 | MAP2K1 | c.15-2A>G (n.15-2A>G) c.81-2A>G (n.81-2A>G) n.517-2A>G n.592-2A>G | dbSNP gnomAD v4 |
| 15 | g.66435025A>T | CA392928854 | MAP2K1 | c.15-2A>T (n.15-2A>T) c.81-2A>T (n.81-2A>T) n.517-2A>T n.592-2A>T | dbSNP |
| 15 | g.66435026G>A | CA392928856 | MAP2K1 | c.15-1G>A (n.15-1G>A) c.81-1G>A (n.81-1G>A) n.517-1G>A n.592-1G>A | dbSNP |
| 15 | g.66435026G>C | CA392928858 | MAP2K1 | c.15-1G>C (n.15-1G>C) c.81-1G>C (n.81-1G>C) n.517-1G>C n.592-1G>C | dbSNP |
| 15 | g.66435026G= | CA2184071707 | MAP2K1 | c.15-1G= (n.15-1G=) c.81-1G= (n.81-1G=) n.517-1G= n.592-1G= | |
| 15 | g.66435026G>T | CA392928860 | MAP2K1 | c.15-1G>T (n.15-1G>T) c.81-1G>T (n.81-1G>T) n.517-1G>T n.592-1G>T | dbSNP gnomAD v4 |
| 15 | g.66435027G>A | CA490855883 | MAP2K1 | c.15G>A (p.Arg5=) c.81G>A (p.Glu27=) n.517G>A n.592G>A | ClinVar dbSNP |
| 15 | g.66435027G>C | CA392928862 | MAP2K1 | c.15G>C (p.Arg5Ser) c.81G>C (p.Glu27Asp) n.517G>C n.592G>C | dbSNP |
| 15 | g.66435027G>T | CA392928863 | MAP2K1 | c.15G>T (p.Arg5Ser) c.81G>T (p.Glu27Asp) n.517G>T n.592G>T | dbSNP |
| 15 | g.66435028A>C | CA392928868 | MAP2K1 | c.16A>C (p.Thr6Pro) c.82A>C (p.Thr28Pro) n.518A>C n.593A>C | |
| 15 | g.66435028A>G | CA392928865 | MAP2K1 | c.16A>G (p.Thr6Ala) c.82A>G (p.Thr28Ala) n.518A>G n.593A>G | dbSNP |
| 15 | g.66435028A>T | CA392928866 | MAP2K1 | c.16A>T (p.Thr6Ser) c.82A>T (p.Thr28Ser) n.518A>T n.593A>T | dbSNP |
| 15 | g.66435029C>A | CA392928870 | MAP2K1 | c.17C>A (p.Thr6Asn) c.83C>A (p.Thr28Asn) n.519C>A n.594C>A | dbSNP gnomAD v4 |
| 15 | g.66435029C>G | CA392928872 | MAP2K1 | c.17C>G (p.Thr6Ser) c.83C>G (p.Thr28Ser) n.519C>G n.594C>G | dbSNP |
| 15 | g.66435029C>T | CA392928873 | MAP2K1 | c.17C>T (p.Thr6Ile) c.83C>T (p.Thr28Ile) n.519C>T n.594C>T | dbSNP |
| 15 | g.66435030C>A | CA490855886 | MAP2K1 | c.18C>A (p.Thr6=) c.84C>A (p.Thr28=) n.520C>A n.595C>A | dbSNP |
| 15 | g.66435030C>G | CA490855884 | MAP2K1 | c.18C>G (p.Thr6=) c.84C>G (p.Thr28=) n.520C>G n.595C>G | dbSNP |
| 15 | g.66435030C>T | CA490855885 | MAP2K1 | c.18C>T (p.Thr6=) c.84C>T (p.Thr28=) n.520C>T n.595C>T | dbSNP |
| 15 | g.66435031A>C | CA392928875 | MAP2K1 | c.19A>C (p.Asn7His) c.85A>C (p.Asn29His) n.521A>C n.596A>C | |
| 15 | g.66435031A>G | CA392928877 | MAP2K1 | c.19A>G (p.Asn7Asp) c.85A>G (p.Asn29Asp) n.521A>G n.596A>G | |
| 15 | g.66435031A>T | CA392928879 | MAP2K1 | c.19A>T (p.Asn7Tyr) c.85A>T (p.Asn29Tyr) n.521A>T n.596A>T | dbSNP |
| 15 | g.66435032A= | CA2184071708 | MAP2K1 | c.20A= (p.Asn7=) c.86A= (p.Asn29=) n.522A= n.597A= | |
| 15 | g.66435032A>C | CA392928882 | MAP2K1 | c.20A>C (p.Asn7Thr) c.86A>C (p.Asn29Thr) n.522A>C n.597A>C | |
| 15 | g.66435032A>G | CA392928883 | MAP2K1 | c.20A>G (p.Asn7Ser) c.86A>G (p.Asn29Ser) n.522A>G n.597A>G | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.66435032A>T | CA392928884 | MAP2K1 | c.20A>T (p.Asn7Ile) c.86A>T (p.Asn29Ile) n.522A>T n.597A>T | dbSNP |
| 15 | g.66435033C>A | CA392928886 | MAP2K1 | c.21C>A (p.Asn7Lys) c.87C>A (p.Asn29Lys) n.523C>A n.598C>A | |
| 15 | g.66435033C= | CA2184071709 | MAP2K1 | c.21C= (p.Asn7=) c.87C= (p.Asn29=) n.523C= n.598C= | |
| 15 | g.66435033C>G | CA392928888 | MAP2K1 | c.21C>G (p.Asn7Lys) c.87C>G (p.Asn29Lys) n.523C>G n.598C>G | dbSNP |
| 15 | g.66435033C>T | CA7623872 | MAP2K1 | c.21C>T (p.Asn7=) c.87C>T (p.Asn29=) n.523C>T n.598C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.66435034T>A | CA392928893 | MAP2K1 | c.22T>A (p.Leu8Met) c.88T>A (p.Leu30Met) n.524T>A n.599T>A | dbSNP |
| 15 | g.66435034T>C | CA490855887 | MAP2K1 | c.22T>C (p.Leu8=) c.88T>C (p.Leu30=) n.524T>C n.599T>C | dbSNP |
| 15 | g.66435034T>G | CA392928891 | MAP2K1 | c.22T>G (p.Leu8Val) c.88T>G (p.Leu30Val) n.524T>G n.599T>G | |
| 15 | g.66435035T>A | CA392928895 | MAP2K1 | c.23T>A (p.Leu8Ter) c.89T>A (p.Leu30Ter) n.525T>A n.600T>A | |
| 15 | g.66435035T>C | CA392928898 | MAP2K1 | c.23T>C (p.Leu8Ser) c.89T>C (p.Leu30Ser) n.525T>C n.600T>C | |
| 15 | g.66435035T>G | CA392928897 | MAP2K1 | c.23T>G (p.Leu8Trp) c.89T>G (p.Leu30Trp) n.525T>G n.600T>G | |
| 15 | g.66435036G>A | CA490855888 | MAP2K1 | c.24G>A (p.Leu8=) c.90G>A (p.Leu30=) n.526G>A n.601G>A | dbSNP gnomAD v4 |
| 15 | g.66435036G>C | CA392928900 | MAP2K1 | c.24G>C (p.Leu8Phe) c.90G>C (p.Leu30Phe) n.526G>C n.601G>C | dbSNP |
| 15 | g.66435036G>T | CA392928901 | MAP2K1 | c.24G>T (p.Leu8Phe) c.90G>T (p.Leu30Phe) n.526G>T n.601G>T | dbSNP |
| 15 | g.66435037del | CA2731110914 | MAP2K1 | c.25del (p.Glu9ArgfsTer10) c.91del (p.Glu31ArgfsTer10) n.527del n.602del | dbSNP |
| 15 | g.66435037G>A | CA392928903 | MAP2K1 | c.25G>A (p.Glu9Lys) c.91G>A (p.Glu31Lys) n.527G>A n.602G>A | dbSNP |
| 15 | g.66435037G>C | CA392928905 | MAP2K1 | c.25G>C (p.Glu9Gln) c.91G>C (p.Glu31Gln) n.527G>C n.602G>C | dbSNP |
| 15 | g.66435037G>T | CA392928906 | MAP2K1 | c.25G>T (p.Glu9Ter) c.91G>T (p.Glu31Ter) n.527G>T n.602G>T | dbSNP |
| 15 | g.66435038A>C | CA392928908 | MAP2K1 | c.26A>C (p.Glu9Ala) c.92A>C (p.Glu31Ala) n.528A>C n.603A>C | |
| 15 | g.66435038A>G | CA392928909 | MAP2K1 | c.26A>G (p.Glu9Gly) c.92A>G (p.Glu31Gly) n.528A>G n.603A>G | dbSNP |
| 15 | g.66435038A>T | CA392928910 | MAP2K1 | c.26A>T (p.Glu9Val) c.92A>T (p.Glu31Val) n.528A>T n.603A>T | dbSNP |
| 15 | g.66435039G>A | CA490855889 | MAP2K1 | c.27G>A (p.Glu9=) c.93G>A (p.Glu31=) n.529G>A n.604G>A | dbSNP |
| 15 | g.66435039G>C | CA392928912 | MAP2K1 | c.27G>C (p.Glu9Asp) c.93G>C (p.Glu31Asp) n.529G>C n.604G>C | dbSNP |
| 15 | g.66435039G= | CA2184071710 | MAP2K1 | c.27G= (p.Glu9=) c.93G= (p.Glu31=) n.529G= n.604G= | |
| 15 | g.66435039G>T | CA392928914 | MAP2K1 | c.27G>T (p.Glu9Asp) c.93G>T (p.Glu31Asp) n.529G>T n.604G>T | |
| 15 | g.66435040G>A | CA392928916 | MAP2K1 | c.28G>A (p.Ala10Thr) c.94G>A (p.Ala32Thr) n.530G>A n.605G>A | dbSNP |
| 15 | g.66435040G>C | CA392928917 | MAP2K1 | c.28G>C (p.Ala10Pro) c.94G>C (p.Ala32Pro) n.530G>C n.605G>C | dbSNP |
| 15 | g.66435040G>T | CA392928919 | MAP2K1 | c.28G>T (p.Ala10Ser) c.94G>T (p.Ala32Ser) n.530G>T n.605G>T | dbSNP |
| 15 | g.66435041C>A | CA392928924 | MAP2K1 | c.29C>A (p.Ala10Asp) c.95C>A (p.Ala32Asp) n.531C>A n.606C>A | dbSNP |
| 15 | g.66435041C= | CA2184071711 | MAP2K1 | c.29C= (p.Ala10=) c.95C= (p.Ala32=) n.531C= n.606C= | |
| 15 | g.66435041C>G | CA392928921 | MAP2K1 | c.29C>G (p.Ala10Gly) c.95C>G (p.Ala32Gly) n.531C>G n.606C>G | dbSNP |
| 15 | g.66435041C>T | CA392928922 | MAP2K1 | c.29C>T (p.Ala10Val) c.95C>T (p.Ala32Val) n.531C>T n.606C>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.66435042C>A | CA490855890 | MAP2K1 | c.30C>A (p.Ala10=) c.96C>A (p.Ala32=) n.532C>A n.607C>A | dbSNP |
| 15 | g.66435042C= | CA2184071712 | MAP2K1 | c.30C= (p.Ala10=) c.96C= (p.Ala32=) n.532C= n.607C= | |
| 15 | g.66435042C>G | CA490855891 | MAP2K1 | c.30C>G (p.Ala10=) c.96C>G (p.Ala32=) n.532C>G n.607C>G | dbSNP |
| 15 | g.66435042C>T | CA7623873 | MAP2K1 | c.30C>T (p.Ala10=) c.96C>T (p.Ala32=) n.532C>T n.607C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.66435043T>A | CA392928927 | MAP2K1 | c.31T>A (p.Leu11Met) c.97T>A (p.Leu33Met) n.533T>A n.608T>A | dbSNP |
| 15 | g.66435043T>C | CA490855892 | MAP2K1 | c.31T>C (p.Leu11=) c.97T>C (p.Leu33=) n.533T>C n.608T>C | dbSNP |
| 15 | g.66435043T>G | CA392928929 | MAP2K1 | c.31T>G (p.Leu11Val) c.97T>G (p.Leu33Val) n.533T>G n.608T>G | |
| 15 | g.66435044T>A | CA392928931 | MAP2K1 | c.32T>A (p.Leu11Ter) c.98T>A (p.Leu33Ter) n.534T>A n.609T>A | |
| 15 | g.66435044T>C | CA392928932 | MAP2K1 | c.32T>C (p.Leu11Ser) c.98T>C (p.Leu33Ser) n.534T>C n.609T>C | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.66435044T>G | CA392928934 | MAP2K1 | c.32T>G (p.Leu11Trp) c.98T>G (p.Leu33Trp) n.534T>G n.609T>G | |
| 15 | g.66435044T= | CA2184071713 | MAP2K1 | c.32T= (p.Leu11=) c.98T= (p.Leu33=) n.534T= n.609T= | |
| 15 | g.66435045G>A | CA490855893 | MAP2K1 | c.33G>A (p.Leu11=) c.99G>A (p.Leu33=) n.535G>A n.610G>A | ClinVar dbSNP |
| 15 | g.66435045G>C | CA392928936 | MAP2K1 | c.33G>C (p.Leu11Phe) c.99G>C (p.Leu33Phe) n.535G>C n.610G>C | dbSNP |
| 15 | g.66435045G>T | CA392928938 | MAP2K1 | c.33G>T (p.Leu11Phe) c.99G>T (p.Leu33Phe) n.535G>T n.610G>T | dbSNP |
| 15 | g.66435046C>A | CA392928939 | MAP2K1 | c.34C>A (p.Gln12Lys) c.100C>A (p.Gln34Lys) n.536C>A n.611C>A | |
| 15 | g.66435046C>G | CA392928941 | MAP2K1 | c.34C>G (p.Gln12Glu) c.100C>G (p.Gln34Glu) n.536C>G n.611C>G | dbSNP |
| 15 | g.66435046C>T | CA392928943 | MAP2K1 | c.34C>T (p.Gln12Ter) c.100C>T (p.Gln34Ter) n.536C>T n.611C>T | dbSNP gnomAD v4 |
| 15 | g.66435047A>C | CA392928947 | MAP2K1 | c.35A>C (p.Gln12Pro) c.101A>C (p.Gln34Pro) n.537A>C n.612A>C | dbSNP |
| 15 | g.66435047A>G | CA392928949 | MAP2K1 | c.35A>G (p.Gln12Arg) c.101A>G (p.Gln34Arg) n.537A>G n.612A>G | dbSNP |
| 15 | g.66435047A>T | CA392928945 | MAP2K1 | c.35A>T (p.Gln12Leu) c.101A>T (p.Gln34Leu) n.537A>T n.612A>T | dbSNP |
| 15 | g.66435048G>A | CA490855894 | MAP2K1 | c.36G>A (p.Gln12=) c.102G>A (p.Gln34=) n.538G>A n.613G>A | dbSNP |
| 15 | g.66435048G>C | CA392928951 | MAP2K1 | c.36G>C (p.Gln12His) c.102G>C (p.Gln34His) n.538G>C n.613G>C | dbSNP |
| 15 | g.66435048G>T | CA392928953 | MAP2K1 | c.36G>T (p.Gln12His) c.102G>T (p.Gln34His) n.538G>T n.613G>T | dbSNP |
| 15 | g.66435049A>C | CA392928955 | MAP2K1 | c.37A>C (p.Lys13Gln) c.103A>C (p.Lys35Gln) n.539A>C n.614A>C | |
| 15 | g.66435049A>G | CA392928956 | MAP2K1 | c.37A>G (p.Lys13Glu) c.103A>G (p.Lys35Glu) n.539A>G n.614A>G | |
| 15 | g.66435049A>T | CA392928958 | MAP2K1 | c.37A>T (p.Lys13Ter) c.103A>T (p.Lys35Ter) n.539A>T n.614A>T | dbSNP |
| 15 | g.66435050A>C | CA392928961 | MAP2K1 | c.38A>C (p.Lys13Thr) c.104A>C (p.Lys35Thr) n.540A>C n.615A>C | |
| 15 | g.66435050A>G | CA392928962 | MAP2K1 | c.38A>G (p.Lys13Arg) c.104A>G (p.Lys35Arg) n.540A>G n.615A>G | gnomAD v4 |
| 15 | g.66435050A>T | CA392928963 | MAP2K1 | c.38A>T (p.Lys13Met) c.104A>T (p.Lys35Met) n.540A>T n.615A>T | |
| 15 | g.66435051G>A | CA490855895 | MAP2K1 | c.39G>A (p.Lys13=) c.105G>A (p.Lys35=) n.541G>A n.616G>A | dbSNP |
| 15 | g.66435051G>C | CA392928965 | MAP2K1 | c.39G>C (p.Lys13Asn) c.105G>C (p.Lys35Asn) n.541G>C n.616G>C | dbSNP |
| 15 | g.66435051G>T | CA392928967 | MAP2K1 | c.39G>T (p.Lys13Asn) c.105G>T (p.Lys35Asn) n.541G>T n.616G>T | |
| 15 | g.66435052A>C | CA392928969 | MAP2K1 | c.40A>C (p.Lys14Gln) c.106A>C (p.Lys36Gln) n.542A>C n.617A>C | |
| 15 | g.66435052A>G | CA392928971 | MAP2K1 | c.40A>G (p.Lys14Glu) c.106A>G (p.Lys36Glu) n.542A>G n.617A>G | dbSNP |
| 15 | g.66435052A>T | CA392928973 | MAP2K1 | c.40A>T (p.Lys14Ter) c.106A>T (p.Lys36Ter) n.542A>T n.617A>T | |
| 15 | g.66435053A>C | CA392928979 | MAP2K1 | c.41A>C (p.Lys14Thr) c.107A>C (p.Lys36Thr) n.543A>C n.618A>C | |
| 15 | g.66435053A>G | CA392928977 | MAP2K1 | c.41A>G (p.Lys14Arg) c.107A>G (p.Lys36Arg) n.543A>G n.618A>G | |
| 15 | g.66435053A>T | CA392928975 | MAP2K1 | c.41A>T (p.Lys14Met) c.107A>T (p.Lys36Met) n.543A>T n.618A>T | dbSNP |
| 15 | g.66435054G>A | CA490855896 | MAP2K1 | c.42G>A (p.Lys14=) c.108G>A (p.Lys36=) n.544G>A n.619G>A | ClinVar dbSNP gnomAD v4 |
| 15 | g.66435054G>C | CA392928981 | MAP2K1 | c.42G>C (p.Lys14Asn) c.108G>C (p.Lys36Asn) n.544G>C n.619G>C | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.66435054G= | CA2184071714 | MAP2K1 | c.42G= (p.Lys14=) c.108G= (p.Lys36=) n.544G= n.619G= | |
| 15 | g.66435054G>T | CA392928983 | MAP2K1 | c.42G>T (p.Lys14Asn) c.108G>T (p.Lys36Asn) n.544G>T n.619G>T | |
| 15 | g.66435055C>A | CA392928985 | MAP2K1 | c.43C>A (p.Leu15Met) c.109C>A (p.Leu37Met) n.545C>A n.620C>A | dbSNP |
| 15 | g.66435055C= | CA2184071715 | MAP2K1 | c.43C= (p.Leu15=) c.109C= (p.Leu37=) n.545C= n.620C= | |
| 15 | g.66435055C>G | CA392928986 | MAP2K1 | c.43C>G (p.Leu15Val) c.109C>G (p.Leu37Val) n.545C>G n.620C>G | dbSNP |
| 15 | g.66435055C>T | CA490855897 | MAP2K1 | c.43C>T (p.Leu15=) c.109C>T (p.Leu37=) n.545C>T n.620C>T | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.66435056T>A | CA392928987 | MAP2K1 | c.44T>A (p.Leu15Gln) c.110T>A (p.Leu37Gln) n.546T>A n.621T>A | |
| 15 | g.66435056T>C | CA392928989 | MAP2K1 | c.44T>C (p.Leu15Pro) c.110T>C (p.Leu37Pro) n.546T>C n.621T>C | |
| 15 | g.66435056T>G | CA392928991 | MAP2K1 | c.44T>G (p.Leu15Arg) c.110T>G (p.Leu37Arg) n.546T>G n.621T>G | |
| 15 | g.66435057G>A | CA490855899 | MAP2K1 | c.45G>A (p.Leu15=) c.111G>A (p.Leu37=) n.547G>A n.622G>A | dbSNP |
| 15 | g.66435057G>C | CA490855900 | MAP2K1 | c.45G>C (p.Leu15=) c.111G>C (p.Leu37=) n.547G>C n.622G>C | dbSNP |
| 15 | g.66435057G>T | CA490855898 | MAP2K1 | c.45G>T (p.Leu15=) c.111G>T (p.Leu37=) n.547G>T n.622G>T | dbSNP |
| 15 | g.66435058G>A | CA392928993 | MAP2K1 | c.46G>A (p.Glu16Lys) c.112G>A (p.Glu38Lys) n.548G>A n.623G>A | dbSNP |
| 15 | g.66435058G>C | CA392928994 | MAP2K1 | c.46G>C (p.Glu16Gln) c.112G>C (p.Glu38Gln) n.548G>C n.623G>C | dbSNP |
| 15 | g.66435058G>T | CA392928996 | MAP2K1 | c.46G>T (p.Glu16Ter) c.112G>T (p.Glu38Ter) n.548G>T n.623G>T | dbSNP |
| 15 | g.66435059del | CA2563258997 | MAP2K1 | c.47del (p.Glu16GlyfsTer3) c.113del (p.Glu38GlyfsTer3) n.549del n.624del | |
| 15 | g.66435059A>C | CA392928998 | MAP2K1 | c.47A>C (p.Glu16Ala) c.113A>C (p.Glu38Ala) n.549A>C n.624A>C | |
| 15 | g.66435059A>G | CA392929000 | MAP2K1 | c.47A>G (p.Glu16Gly) c.113A>G (p.Glu38Gly) n.549A>G n.624A>G | dbSNP |
| 15 | g.66435059A>T | CA392929001 | MAP2K1 | c.47A>T (p.Glu16Val) c.113A>T (p.Glu38Val) n.549A>T n.624A>T | dbSNP |
| 15 | g.66435060G>A | CA490855901 | MAP2K1 | c.48G>A (p.Glu16=) c.114G>A (p.Glu38=) n.550G>A n.625G>A | dbSNP |
| 15 | g.66435060G>C | CA392929003 | MAP2K1 | c.48G>C (p.Glu16Asp) c.114G>C (p.Glu38Asp) n.550G>C n.625G>C | dbSNP |
| 15 | g.66435060G>T | CA392929004 | MAP2K1 | c.48G>T (p.Glu16Asp) c.114G>T (p.Glu38Asp) n.550G>T n.625G>T | |
| 15 | g.66435061G>A | CA392929005 | MAP2K1 | c.49G>A (p.Glu17Lys) c.115G>A (p.Glu39Lys) n.551G>A n.626G>A | dbSNP |
| 15 | g.66435061G>C | CA392929008 | MAP2K1 | c.49G>C (p.Glu17Gln) c.115G>C (p.Glu39Gln) n.551G>C n.626G>C | dbSNP |
| 15 | g.66435061G>T | CA392929006 | MAP2K1 | c.49G>T (p.Glu17Ter) c.115G>T (p.Glu39Ter) n.551G>T n.626G>T | |
| 15 | g.66435062A>C | CA392929010 | MAP2K1 | c.50A>C (p.Glu17Ala) c.116A>C (p.Glu39Ala) n.552A>C n.627A>C | |
| 15 | g.66435062A>G | CA392929011 | MAP2K1 | c.50A>G (p.Glu17Gly) c.116A>G (p.Glu39Gly) n.552A>G n.627A>G | dbSNP |
| 15 | g.66435062A>T | CA392929013 | MAP2K1 | c.50A>T (p.Glu17Val) c.116A>T (p.Glu39Val) n.552A>T n.627A>T | dbSNP |
| 15 | g.66435063G>A | CA490855902 | MAP2K1 | c.51G>A (p.Glu17=) c.117G>A (p.Glu39=) n.553G>A n.628G>A | dbSNP gnomAD v4 |
| 15 | g.66435063G>C | CA392929014 | MAP2K1 | c.51G>C (p.Glu17Asp) c.117G>C (p.Glu39Asp) n.553G>C n.628G>C | dbSNP |
| 15 | g.66435063G>T | CA392929015 | MAP2K1 | c.51G>T (p.Glu17Asp) c.117G>T (p.Glu39Asp) n.553G>T n.628G>T | |
| 15 | g.66435063_66435064delinsGC | CA2184071716 | MAP2K1 | c.51_52delinsGC (p.Glu17=) c.117_118delinsGC (p.Glu39=) n.553_554delinsGC n.628_629delinsGC | |
| 15 | g.66435064del | CA7623874 | MAP2K1 | c.52del (p.Leu18Ter) c.118del (p.Leu40Ter) n.554del n.629del | dbSNP ExAC gnomAD v2 |
| 15 | g.66435064C>A | CA392929017 | MAP2K1 | c.52C>A (p.Leu18Ile) c.118C>A (p.Leu40Ile) n.554C>A n.629C>A | dbSNP |
| 15 | g.66435064C= | CA2184071717 | MAP2K1 | c.52C= (p.Leu18=) c.118C= (p.Leu40=) n.554C= n.629C= | |
| 15 | g.66435064C>G | CA392929019 | MAP2K1 | c.52C>G (p.Leu18Val) c.118C>G (p.Leu40Val) n.554C>G n.629C>G | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.66435064C>T | CA490855903 | MAP2K1 | c.52C>T (p.Leu18=) c.118C>T (p.Leu40=) n.554C>T n.629C>T | gnomAD v4 |
| 15 | g.66435064dup | CA2629081329 | MAP2K1 | c.52dup (p.Leu18ProfsTer4) c.118dup (p.Leu40ProfsTer4) n.554dup n.629dup | gnomAD v4 |
| 15 | g.66435065T>A | CA392929021 | MAP2K1 | c.53T>A (p.Leu18Gln) c.119T>A (p.Leu40Gln) n.555T>A n.630T>A | |
| 15 | g.66435065T>C | CA392929023 | MAP2K1 | c.53T>C (p.Leu18Pro) c.119T>C (p.Leu40Pro) n.555T>C n.630T>C | dbSNP |
| 15 | g.66435065T>G | CA392929025 | MAP2K1 | c.53T>G (p.Leu18Arg) c.119T>G (p.Leu40Arg) n.555T>G n.630T>G | |
| 15 | g.66435066A>C | CA490855905 | MAP2K1 | c.54A>C (p.Leu18=) c.120A>C (p.Leu40=) n.556A>C n.631A>C | |
| 15 | g.66435066A>G | CA490855904 | MAP2K1 | c.54A>G (p.Leu18=) c.120A>G (p.Leu40=) n.556A>G n.631A>G | dbSNP |
| 15 | g.66435066A>T | CA490855906 | MAP2K1 | c.54A>T (p.Leu18=) c.120A>T (p.Leu40=) n.556A>T n.631A>T | dbSNP |
| 15 | g.66435067G>A | CA392929031 | MAP2K1 | c.55G>A (p.Glu19Lys) c.121G>A (p.Glu41Lys) n.557G>A n.632G>A | dbSNP |
| 15 | g.66435067G>C | CA392929029 | MAP2K1 | c.55G>C (p.Glu19Gln) c.121G>C (p.Glu41Gln) n.557G>C n.632G>C | dbSNP |
| 15 | g.66435067G>T | CA392929027 | MAP2K1 | c.55G>T (p.Glu19Ter) c.121G>T (p.Glu41Ter) n.557G>T n.632G>T | |
| 15 | g.66435068A>C | CA392929034 | MAP2K1 | c.56A>C (p.Glu19Ala) c.122A>C (p.Glu41Ala) n.558A>C n.633A>C | |
| 15 | g.66435068A>G | CA392929035 | MAP2K1 | c.56A>G (p.Glu19Gly) c.122A>G (p.Glu41Gly) n.558A>G n.633A>G | dbSNP |
| 15 | g.66435068A>T | CA392929036 | MAP2K1 | c.56A>T (p.Glu19Val) c.122A>T (p.Glu41Val) n.558A>T n.633A>T | dbSNP |
| 15 | g.66435071_66435118del | CA645570529 | MAP2K1 | c.59_106del (p.Leu20_Lys35del) c.125_172del (p.Leu42_Lys57del) n.561_608del n.636_683del | COSMIC |
| 15 | g.66435069G>A | CA490855907 | MAP2K1 | c.57G>A (p.Glu19=) c.123G>A (p.Glu41=) n.559G>A n.634G>A | dbSNP |
| 15 | g.66435069G>C | CA392929038 | MAP2K1 | c.57G>C (p.Glu19Asp) c.123G>C (p.Glu41Asp) n.559G>C n.634G>C | dbSNP gnomAD v4 |
| 15 | g.66435069G= | CA2184071718 | MAP2K1 | c.57G= (p.Glu19=) c.123G= (p.Glu41=) n.559G= n.634G= | |
| 15 | g.66435069G>T | CA392929040 | MAP2K1 | c.57G>T (p.Glu19Asp) c.123G>T (p.Glu41Asp) n.559G>T n.634G>T | dbSNP |
| 15 | g.66435070C>A | CA392929042 | MAP2K1 | c.58C>A (p.Leu20Ile) c.124C>A (p.Leu42Ile) n.560C>A n.635C>A | |
| 15 | g.66435070C= | CA2184071719 | MAP2K1 | c.58C= (p.Leu20=) c.124C= (p.Leu42=) n.560C= n.635C= | |
| 15 | g.66435070C>G | CA392929043 | MAP2K1 | c.58C>G (p.Leu20Val) c.124C>G (p.Leu42Val) n.560C>G n.635C>G | dbSNP |
| 15 | g.66435070C>T | CA279993 | MAP2K1 | c.58C>T (p.Leu20Phe) c.124C>T (p.Leu42Phe) n.560C>T n.635C>T | ClinVar dbSNP COSMIC |
| 15 | g.66435071T>A | CA392929046 | MAP2K1 | c.59T>A (p.Leu20His) c.125T>A (p.Leu42His) n.561T>A n.636T>A | COSMIC |
| 15 | g.66435071T>C | CA392929048 | MAP2K1 | c.59T>C (p.Leu20Pro) c.125T>C (p.Leu42Pro) n.561T>C n.636T>C | |
| 15 | g.66435071T>G | CA392929050 | MAP2K1 | c.59T>G (p.Leu20Arg) c.125T>G (p.Leu42Arg) n.561T>G n.636T>G | ClinVar dbSNP |
| 15 | g.66435071T= | CA2184071721 | MAP2K1 | c.59T= (p.Leu20=) c.125T= (p.Leu42=) n.561T= n.636T= | |
| 15 | g.66435072dup | CA2731112622 | MAP2K1 | c.60dup (p.Asp21Ter) c.126dup (p.Asp43Ter) n.562dup n.637dup | dbSNP |
| 15 | g.66435071_66435074delinsTTGA | CA2184071720 | MAP2K1 | c.59_62delinsTTGA (p.Leu20=) c.125_128delinsTTGA (p.Leu42=) n.561_564delinsTTGA n.636_639delinsTTGA | |
| 15 | g.66435072T>A | CA490855909 | MAP2K1 | c.60T>A (p.Leu20=) c.126T>A (p.Leu42=) n.562T>A n.637T>A | dbSNP |
| 15 | g.66435072T>C | CA7623875 | MAP2K1 | c.60T>C (p.Leu20=) c.126T>C (p.Leu42=) n.562T>C n.637T>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.66435072T>G | CA490855908 | MAP2K1 | c.60T>G (p.Leu20=) c.126T>G (p.Leu42=) n.562T>G n.637T>G | dbSNP |
| 15 | g.66435072T= | CA2184071722 | MAP2K1 | c.60T= (p.Leu20=) c.126T= (p.Leu42=) n.562T= n.637T= | |
| 15 | g.66435075_66435077del | CA658656490 | MAP2K1 | c.63_65del (p.Asp21del) c.129_131del (p.Asp43del) n.565_567del n.640_642del | ClinVar dbSNP |
| 15 | g.66435073G>A | CA392929056 | MAP2K1 | c.61G>A (p.Asp21Asn) c.127G>A (p.Asp43Asn) n.563G>A n.638G>A | dbSNP |
| 15 | g.66435073G>C | CA392929054 | MAP2K1 | c.61G>C (p.Asp21His) c.127G>C (p.Asp43His) n.563G>C n.638G>C | dbSNP |
| 15 | g.66435073G>T | CA392929053 | MAP2K1 | c.61G>T (p.Asp21Tyr) c.127G>T (p.Asp43Tyr) n.563G>T n.638G>T | dbSNP |
| 15 | g.66435074A>C | CA392929058 | MAP2K1 | c.62A>C (p.Asp21Ala) c.128A>C (p.Asp43Ala) n.564A>C n.639A>C | |
| 15 | g.66435074A>G | CA392929060 | MAP2K1 | c.62A>G (p.Asp21Gly) c.128A>G (p.Asp43Gly) n.564A>G n.639A>G | dbSNP |
| 15 | g.66435074A>T | CA392929062 | MAP2K1 | c.62A>T (p.Asp21Val) c.128A>T (p.Asp43Val) n.564A>T n.639A>T | dbSNP |
| 15 | g.66435075T>A | CA392929064 | MAP2K1 | c.63T>A (p.Asp21Glu) c.129T>A (p.Asp43Glu) n.565T>A n.640T>A | |
| 15 | g.66435075T>C | CA490855910 | MAP2K1 | c.63T>C (p.Asp21=) c.129T>C (p.Asp43=) n.565T>C n.640T>C | |
| 15 | g.66435075T>G | CA392929065 | MAP2K1 | c.63T>G (p.Asp21Glu) c.129T>G (p.Asp43Glu) n.565T>G n.640T>G | |
| 15 | g.66435076_66435108del | CA2573151054 | MAP2K1 | c.64_96del (p.Glu22_Leu32del) c.130_162del (p.Glu44_Leu54del) n.566_598del n.641_673del | ClinVar dbSNP |
| 15 | g.66435076G>A | CA392929068 | MAP2K1 | c.64G>A (p.Glu22Lys) c.130G>A (p.Glu44Lys) n.566G>A n.641G>A | dbSNP |
| 15 | g.66435076G>C | CA392929069 | MAP2K1 | c.64G>C (p.Glu22Gln) c.130G>C (p.Glu44Gln) n.566G>C n.641G>C | dbSNP |
| 15 | g.66435076G>T | CA392929071 | MAP2K1 | c.64G>T (p.Glu22Ter) c.130G>T (p.Glu44Ter) n.566G>T n.641G>T | dbSNP gnomAD v4 |
| 15 | g.66435077A= | CA2184071723 | MAP2K1 | c.65A= (p.Glu22=) c.131A= (p.Glu44=) n.567A= n.642A= | |
| 15 | g.66435077A>C | CA392929073 | MAP2K1 | c.65A>C (p.Glu22Ala) c.131A>C (p.Glu44Ala) n.567A>C n.642A>C | |
| 15 | g.66435077A>G | CA392929075 | MAP2K1 | c.65A>G (p.Glu22Gly) c.131A>G (p.Glu44Gly) n.567A>G n.642A>G | dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 15 | g.66435077A>T | CA392929077 | MAP2K1 | c.65A>T (p.Glu22Val) c.131A>T (p.Glu44Val) n.567A>T n.642A>T | dbSNP |
| 15 | g.66435078G>A | CA490855911 | MAP2K1 | c.66G>A (p.Glu22=) c.132G>A (p.Glu44=) n.568G>A n.643G>A | dbSNP gnomAD v4 |
| 15 | g.66435078G>C | CA392929079 | MAP2K1 | c.66G>C (p.Glu22Asp) c.132G>C (p.Glu44Asp) n.568G>C n.643G>C | dbSNP |
| 15 | g.66435078G= | CA2184071724 | MAP2K1 | c.66G= (p.Glu22=) c.132G= (p.Glu44=) n.568G= n.643G= | |
| 15 | g.66435078G>T | CA392929080 | MAP2K1 | c.66G>T (p.Glu22Asp) c.132G>T (p.Glu44Asp) n.568G>T n.643G>T | |
| 15 | g.66435079C>A | CA392929086 | MAP2K1 | c.67C>A (p.Gln23Lys) c.133C>A (p.Gln45Lys) n.569C>A n.644C>A | |
| 15 | g.66435079C>G | CA392929083 | MAP2K1 | c.67C>G (p.Gln23Glu) c.133C>G (p.Gln45Glu) n.569C>G n.644C>G | dbSNP |
| 15 | g.66435079C>T | CA392929084 | MAP2K1 | c.67C>T (p.Gln23Ter) c.133C>T (p.Gln45Ter) n.569C>T n.644C>T | dbSNP |
| 15 | g.66435080A>C | CA392929087 | MAP2K1 | c.68A>C (p.Gln23Pro) c.134A>C (p.Gln45Pro) n.570A>C n.645A>C | |
| 15 | g.66435080A>G | CA392929089 | MAP2K1 | c.68A>G (p.Gln23Arg) c.134A>G (p.Gln45Arg) n.570A>G n.645A>G | |
| 15 | g.66435080A>T | CA392929091 | MAP2K1 | c.68A>T (p.Gln23Leu) c.134A>T (p.Gln45Leu) n.570A>T n.645A>T | dbSNP |
| 15 | g.66435081G>A | CA490855912 | MAP2K1 | c.69G>A (p.Gln23=) c.135G>A (p.Gln45=) n.571G>A n.646G>A | dbSNP gnomAD v4 |
| 15 | g.66435081G>C | CA392929092 | MAP2K1 | c.69G>C (p.Gln23His) c.135G>C (p.Gln45His) n.571G>C n.646G>C | dbSNP |
| 15 | g.66435081G= | CA2184071725 | MAP2K1 | c.69G= (p.Gln23=) c.135G= (p.Gln45=) n.571G= n.646G= | |
| 15 | g.66435081G>T | CA392929095 | MAP2K1 | c.69G>T (p.Gln23His) c.135G>T (p.Gln45His) n.571G>T n.646G>T | ClinVar dbSNP gnomAD v4 |
| 15 | g.66435082C>A | CA392929097 | MAP2K1 | c.70C>A (p.Gln24Lys) c.136C>A (p.Gln46Lys) n.572C>A n.647C>A | |
| 15 | g.66435082C>G | CA392929098 | MAP2K1 | c.70C>G (p.Gln24Glu) c.136C>G (p.Gln46Glu) n.572C>G n.647C>G | dbSNP |
| 15 | g.66435082C>T | CA392929101 | MAP2K1 | c.70C>T (p.Gln24Ter) c.136C>T (p.Gln46Ter) n.572C>T n.647C>T | dbSNP |
| 15 | g.66435083A= | CA2184071726 | MAP2K1 | c.71A= (p.Gln24=) c.137A= (p.Gln46=) n.573A= n.648A= | |
| 15 | g.66435083A>C | CA392929103 | MAP2K1 | c.71A>C (p.Gln24Pro) c.137A>C (p.Gln46Pro) n.573A>C n.648A>C | |
| 15 | g.66435083A>G | CA392929104 | MAP2K1 | c.71A>G (p.Gln24Arg) c.137A>G (p.Gln46Arg) n.573A>G n.648A>G | |
| 15 | g.66435083A>T | CA392929105 | MAP2K1 | c.71A>T (p.Gln24Leu) c.137A>T (p.Gln46Leu) n.573A>T n.648A>T | ClinVar dbSNP |
| 15 | g.66435084del | CA2697549135 | MAP2K1 | c.72del (p.Gln24HisfsTer18) c.138del (p.Gln46HisfsTer18) n.574del n.649del | ClinVar |
| 15 | g.66435084G>A | CA490855913 | MAP2K1 | c.72G>A (p.Gln24=) c.138G>A (p.Gln46=) n.574G>A n.649G>A | dbSNP |
| 15 | g.66435084G>C | CA392929117 | MAP2K1 | c.72G>C (p.Gln24His) c.138G>C (p.Gln46His) n.574G>C n.649G>C | dbSNP |
| 15 | g.66435084G>T | CA392929118 | MAP2K1 | c.72G>T (p.Gln24His) c.138G>T (p.Gln46His) n.574G>T n.649G>T | |
| 15 | g.66435085C>A | CA490855914 | MAP2K1 | c.73C>A (p.Arg25=) c.139C>A (p.Arg47=) n.575C>A n.650C>A | ClinVar dbSNP |
| 15 | g.66435085C= | CA2184071727 | MAP2K1 | c.73C= (p.Arg25=) c.139C= (p.Arg47=) n.575C= n.650C= | |
| 15 | g.66435085C>G | CA392929120 | MAP2K1 | c.73C>G (p.Arg25Gly) c.139C>G (p.Arg47Gly) n.575C>G n.650C>G | dbSNP |
| 15 | g.66435085C>T | CA271640690 | MAP2K1 | c.73C>T (p.Arg25Ter) c.139C>T (p.Arg47Ter) n.575C>T n.650C>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.66435086G>A | CA392929123 | MAP2K1 | c.74G>A (p.Arg25Gln) c.140G>A (p.Arg47Gln) n.576G>A n.651G>A | ClinVar dbSNP gnomAD v4 COSMIC |
| 15 | g.66435086G>C | CA392929127 | MAP2K1 | c.74G>C (p.Arg25Pro) c.140G>C (p.Arg47Pro) n.576G>C n.651G>C | dbSNP |
| 15 | g.66435086G= | CA2184071728 | MAP2K1 | c.74G= (p.Arg25=) c.140G= (p.Arg47=) n.576G= n.651G= | |
| 15 | g.66435086G>T | CA392929125 | MAP2K1 | c.74G>T (p.Arg25Leu) c.140G>T (p.Arg47Leu) n.576G>T n.651G>T | |
| 15 | g.66435087A= | CA2184071729 | MAP2K1 | c.75A= (p.Arg25=) c.141A= (p.Arg47=) n.577A= n.652A= | |
| 15 | g.66435087A>C | CA490855917 | MAP2K1 | c.75A>C (p.Arg25=) c.141A>C (p.Arg47=) n.577A>C n.652A>C | |
| 15 | g.66435087A>G | CA490855916 | MAP2K1 | c.75A>G (p.Arg25=) c.141A>G (p.Arg47=) n.577A>G n.652A>G | dbSNP |
| 15 | g.66435087A>T | CA490855915 | MAP2K1 | c.75A>T (p.Arg25=) c.141A>T (p.Arg47=) n.577A>T n.652A>T | dbSNP |
| 15 | g.66435088A= | CA2184071730 | MAP2K1 | c.76A= (p.Lys26=) c.142A= (p.Lys48=) n.578A= n.653A= | |
| 15 | g.66435088A>C | CA392929129 | MAP2K1 | c.76A>C (p.Lys26Gln) c.142A>C (p.Lys48Gln) n.578A>C n.653A>C | |
| 15 | g.66435088A>G | CA392929133 | MAP2K1 | c.76A>G (p.Lys26Glu) c.142A>G (p.Lys48Glu) n.578A>G n.653A>G | dbSNP |
| 15 | g.66435088A>T | CA392929131 | MAP2K1 | c.76A>T (p.Lys26Ter) c.142A>T (p.Lys48Ter) n.578A>T n.653A>T | dbSNP |
| 15 | g.66435089A>C | CA392929134 | MAP2K1 | c.77A>C (p.Lys26Thr) c.143A>C (p.Lys48Thr) n.579A>C n.654A>C | dbSNP |
| 15 | g.66435089A>G | CA392929136 | MAP2K1 | c.77A>G (p.Lys26Arg) c.143A>G (p.Lys48Arg) n.579A>G n.654A>G | dbSNP |
| 15 | g.66435089A>T | CA392929138 | MAP2K1 | c.77A>T (p.Lys26Met) c.143A>T (p.Lys48Met) n.579A>T n.654A>T | dbSNP |
| 15 | g.66435090G>A | CA490855918 | MAP2K1 | c.78G>A (p.Lys26=) c.144G>A (p.Lys48=) n.580G>A n.655G>A | dbSNP |
| 15 | g.66435090G>C | CA392929139 | MAP2K1 | c.78G>C (p.Lys26Asn) c.144G>C (p.Lys48Asn) n.580G>C n.655G>C | dbSNP |
| 15 | g.66435090G>T | CA392929140 | MAP2K1 | c.78G>T (p.Lys26Asn) c.144G>T (p.Lys48Asn) n.580G>T n.655G>T | |
| 15 | g.66435090_66435091delinsA | CA2695220905 | MAP2K1 | c.78_79delinsA (p.Arg27AlafsTer15) c.144_145delinsA (p.Arg49AlafsTer15) n.580_581delinsA n.655_656delinsA | |
| 15 | g.66435091C>A | CA392929141 | MAP2K1 | c.79C>A (p.Arg27Ser) c.145C>A (p.Arg49Ser) n.581C>A n.656C>A | dbSNP |
| 15 | g.66435091C>G | CA392929143 | MAP2K1 | c.79C>G (p.Arg27Gly) c.145C>G (p.Arg49Gly) n.581C>G n.656C>G | dbSNP |
| 15 | g.66435091C>T | CA392929144 | MAP2K1 | c.79C>T (p.Arg27Cys) c.145C>T (p.Arg49Cys) n.581C>T n.656C>T | dbSNP gnomAD v4 COSMIC |
| 15 | g.66435092G>A | CA271640694 | MAP2K1 | c.80G>A (p.Arg27His) c.146G>A (p.Arg49His) n.582G>A n.657G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 15 | g.66435092G>C | CA392929148 | MAP2K1 | c.80G>C (p.Arg27Pro) c.146G>C (p.Arg49Pro) n.582G>C n.657G>C | |
| 15 | g.66435092G= | CA2184071731 | MAP2K1 | c.80G= (p.Arg27=) c.146G= (p.Arg49=) n.582G= n.657G= | |
| 15 | g.66435092G>T | CA392929149 | MAP2K1 | c.80G>T (p.Arg27Leu) c.146G>T (p.Arg49Leu) n.582G>T n.657G>T | COSMIC |
| 15 | g.66435093C>A | CA7623876 | MAP2K1 | c.81C>A (p.Arg27=) c.147C>A (p.Arg49=) n.583C>A n.658C>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.66435093C= | CA2184071732 | MAP2K1 | c.81C= (p.Arg27=) c.147C= (p.Arg49=) n.583C= n.658C= | |
| 15 | g.66435093C>G | CA490855920 | MAP2K1 | c.81C>G (p.Arg27=) c.147C>G (p.Arg49=) n.583C>G n.658C>G | |
| 15 | g.66435093C>T | CA490855919 | MAP2K1 | c.81C>T (p.Arg27=) c.147C>T (p.Arg49=) n.583C>T n.658C>T | dbSNP |
| 15 | g.66435094C>A | CA392929157 | MAP2K1 | c.82C>A (p.Leu28Ile) c.148C>A (p.Leu50Ile) n.584C>A n.659C>A | dbSNP |
| 15 | g.66435094C= | CA2184071733 | MAP2K1 | c.82C= (p.Leu28=) c.148C= (p.Leu50=) n.584C= n.659C= | |
| 15 | g.66435094C>G | CA392929153 | MAP2K1 | c.82C>G (p.Leu28Val) c.148C>G (p.Leu50Val) n.584C>G n.659C>G | dbSNP |
| 15 | g.66435094C>T | CA392929155 | MAP2K1 | c.82C>T (p.Leu28Phe) c.148C>T (p.Leu50Phe) n.584C>T n.659C>T | dbSNP |
| 15 | g.66435095T>A | CA392929159 | MAP2K1 | c.83T>A (p.Leu28His) c.149T>A (p.Leu50His) n.585T>A n.660T>A | dbSNP |
| 15 | g.66435095T>C | CA392929161 | MAP2K1 | c.83T>C (p.Leu28Pro) c.149T>C (p.Leu50Pro) n.585T>C n.660T>C | ClinVar dbSNP |
| 15 | g.66435095T>G | CA392929163 | MAP2K1 | c.83T>G (p.Leu28Arg) c.149T>G (p.Leu50Arg) n.585T>G n.660T>G | |
| 15 | g.66435096T>A | CA490855921 | MAP2K1 | c.84T>A (p.Leu28=) c.150T>A (p.Leu50=) n.586T>A n.661T>A | |
| 15 | g.66435096T>C | CA490855923 | MAP2K1 | c.84T>C (p.Leu28=) c.150T>C (p.Leu50=) n.586T>C n.661T>C | dbSNP |
| 15 | g.66435096T>G | CA490855922 | MAP2K1 | c.84T>G (p.Leu28=) c.150T>G (p.Leu50=) n.586T>G n.661T>G | |
| 15 | g.66435096T= | CA2184071734 | MAP2K1 | c.84T= (p.Leu28=) c.150T= (p.Leu50=) n.586T= n.661T= | |
| 15 | g.66435097G>A | CA392929164 | MAP2K1 | c.85G>A (p.Glu29Lys) c.151G>A (p.Glu51Lys) n.587G>A n.662G>A | dbSNP |
| 15 | g.66435097G>C | CA392929165 | MAP2K1 | c.85G>C (p.Glu29Gln) c.151G>C (p.Glu51Gln) n.587G>C n.662G>C | dbSNP |
| 15 | g.66435097G>T | CA392929167 | MAP2K1 | c.85G>T (p.Glu29Ter) c.151G>T (p.Glu51Ter) n.587G>T n.662G>T | |
| 15 | g.66435098A>C | CA392929169 | MAP2K1 | c.86A>C (p.Glu29Ala) c.152A>C (p.Glu51Ala) n.588A>C n.663A>C | |
| 15 | g.66435098A>G | CA392929171 | MAP2K1 | c.86A>G (p.Glu29Gly) c.152A>G (p.Glu51Gly) n.588A>G n.663A>G | |
| 15 | g.66435098A>T | CA392929172 | MAP2K1 | c.86A>T (p.Glu29Val) c.152A>T (p.Glu51Val) n.588A>T n.663A>T | |
| 15 | g.66435099G>A | CA490855924 | MAP2K1 | c.87G>A (p.Glu29=) c.153G>A (p.Glu51=) n.589G>A n.664G>A | ClinVar dbSNP gnomAD v4 |
| 15 | g.66435099G>C | CA392929174 | MAP2K1 | c.87G>C (p.Glu29Asp) c.153G>C (p.Glu51Asp) n.589G>C n.664G>C | dbSNP |
| 15 | g.66435099G= | CA2184071735 | MAP2K1 | c.87G= (p.Glu29=) c.153G= (p.Glu51=) n.589G= n.664G= | |
| 15 | g.66435099G>T | CA392929176 | MAP2K1 | c.87G>T (p.Glu29Asp) c.153G>T (p.Glu51Asp) n.589G>T n.664G>T | dbSNP |
| 15 | g.66435100G>A | CA392929181 | MAP2K1 | c.88G>A (p.Ala30Thr) c.154G>A (p.Ala52Thr) n.590G>A n.665G>A | dbSNP gnomAD v4 |
| 15 | g.66435100G>C | CA392929179 | MAP2K1 | c.88G>C (p.Ala30Pro) c.154G>C (p.Ala52Pro) n.590G>C n.665G>C | dbSNP |
| 15 | g.66435100G>T | CA392929178 | MAP2K1 | c.88G>T (p.Ala30Ser) c.154G>T (p.Ala52Ser) n.590G>T n.665G>T | |
| 15 | g.66435101C>A | CA392929186 | MAP2K1 | c.89C>A (p.Ala30Asp) c.155C>A (p.Ala52Asp) n.591C>A n.666C>A | dbSNP |
| 15 | g.66435101C>G | CA392929183 | MAP2K1 | c.89C>G (p.Ala30Gly) c.155C>G (p.Ala52Gly) n.591C>G n.666C>G | dbSNP |
| 15 | g.66435101C>T | CA392929185 | MAP2K1 | c.89C>T (p.Ala30Val) c.155C>T (p.Ala52Val) n.591C>T n.666C>T | dbSNP |
| 15 | g.66435102C>A | CA490855925 | MAP2K1 | c.90C>A (p.Ala30=) c.156C>A (p.Ala52=) n.592C>A n.667C>A | |
| 15 | g.66435102C= | CA2184071736 | MAP2K1 | c.90C= (p.Ala30=) c.156C= (p.Ala52=) n.592C= n.667C= | |
| 15 | g.66435102C>G | CA490855926 | MAP2K1 | c.90C>G (p.Ala30=) c.156C>G (p.Ala52=) n.592C>G n.667C>G | ClinVar dbSNP |
| 15 | g.66435102C>T | CA176700 | MAP2K1 | c.90C>T (p.Ala30=) c.156C>T (p.Ala52=) n.592C>T n.667C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.66435103T>A | CA16602882 | MAP2K1 | c.91T>A (p.Phe31Ile) c.157T>A (p.Phe53Ile) n.593T>A n.668T>A | ClinVar dbSNP COSMIC |
| 15 | g.66435103T>C | CA16602452 | MAP2K1 | c.91T>C (p.Phe31Leu) c.157T>C (p.Phe53Leu) n.593T>C n.668T>C | ClinVar dbSNP COSMIC |
| 15 | g.66435103T>G | CA16602881 | MAP2K1 | c.91T>G (p.Phe31Val) c.157T>G (p.Phe53Val) n.593T>G n.668T>G | ClinVar dbSNP COSMIC |
| 15 | g.66435103T= | CA2184071737 | MAP2K1 | c.91T= (p.Phe31=) c.157T= (p.Phe53=) n.593T= n.668T= | |
| 15 | g.66435104T>A | CA392929195 | MAP2K1 | c.92T>A (p.Phe31Tyr) c.158T>A (p.Phe53Tyr) n.594T>A n.669T>A | dbSNP COSMIC |
| 15 | g.66435104T>C | CA279966 | MAP2K1 | c.92T>C (p.Phe31Ser) c.158T>C (p.Phe53Ser) n.594T>C n.669T>C | ClinVar dbSNP |
| 15 | g.66435104T>G | CA392929193 | MAP2K1 | c.92T>G (p.Phe31Cys) c.158T>G (p.Phe53Cys) n.594T>G n.669T>G | dbSNP COSMIC |
| 15 | g.66435104T= | CA2184071738 | MAP2K1 | c.92T= (p.Phe31=) c.158T= (p.Phe53=) n.594T= n.669T= | |
| 15 | g.66435106_66435108del | CA2695220906 | MAP2K1 | c.94_96del (p.Leu32del) c.160_162del (p.Leu54del) n.596_598del n.671_673del | |
| 15 | g.66435105_66435134del | CA2580618255 | MAP2K1 | c.93_122del (p.Phe31_Glu40del) c.159_188del (p.Phe53_Glu62del) n.595_624del n.670_699del | |
| 15 | g.66435105T>A | CA392929197 | MAP2K1 | c.93T>A (p.Phe31Leu) c.159T>A (p.Phe53Leu) n.595T>A n.670T>A | dbSNP COSMIC |
| 15 | g.66435105T>C | CA490855927 | MAP2K1 | c.93T>C (p.Phe31=) c.159T>C (p.Phe53=) n.595T>C n.670T>C | dbSNP |
| 15 | g.66435105T>G | CA16602880 | MAP2K1 | c.93T>G (p.Phe31Leu) c.159T>G (p.Phe53Leu) n.595T>G n.670T>G | ClinVar dbSNP COSMIC |
| 15 | g.66435105T= | CA2184071739 | MAP2K1 | c.93T= (p.Phe31=) c.159T= (p.Phe53=) n.595T= n.670T= | |
| 15 | g.66435105_66435119del | CA645570532 | MAP2K1 | c.93_107del (p.Phe31_Gln36delinsLeu) c.159_173del (p.Phe53_Gln58delinsLeu) n.595_609del n.670_684del | COSMIC |
| 15 | g.66435106C>A | CA392929198 | MAP2K1 | c.94C>A (p.Leu32Ile) c.160C>A (p.Leu54Ile) n.596C>A n.671C>A | |
| 15 | g.66435106C>G | CA392929200 | MAP2K1 | c.94C>G (p.Leu32Val) c.160C>G (p.Leu54Val) n.596C>G n.671C>G | gnomAD v4 |
| 15 | g.66435106C>T | CA392929202 | MAP2K1 | c.94C>T (p.Leu32Phe) c.160C>T (p.Leu54Phe) n.596C>T n.671C>T | |
| 15 | g.66435107T>A | CA392929204 | MAP2K1 | c.95T>A (p.Leu32His) c.161T>A (p.Leu54His) n.597T>A n.672T>A | dbSNP |
| 15 | g.66435107T>C | CA392929208 | MAP2K1 | c.95T>C (p.Leu32Pro) c.161T>C (p.Leu54Pro) n.597T>C n.672T>C | ClinVar dbSNP COSMIC |
| 15 | g.66435107T>G | CA392929206 | MAP2K1 | c.95T>G (p.Leu32Arg) c.161T>G (p.Leu54Arg) n.597T>G n.672T>G | |
| 15 | g.66435108T>A | CA490855930 | MAP2K1 | c.96T>A (p.Leu32=) c.162T>A (p.Leu54=) n.598T>A n.673T>A | |
| 15 | g.66435108T>C | CA490855931 | MAP2K1 | c.96T>C (p.Leu32=) c.162T>C (p.Leu54=) n.598T>C n.673T>C | |
| 15 | g.66435108T>G | CA7623877 | MAP2K1 | c.96T>G (p.Leu32=) c.162T>G (p.Leu54=) n.598T>G n.673T>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.66435108T= | CA2184071740 | MAP2K1 | c.96T= (p.Leu32=) c.162T= (p.Leu54=) n.598T= n.673T= | |
| 15 | g.66435109del | CA2731113720 | MAP2K1 | c.97del (p.Thr33ProfsTer9) c.163del (p.Thr55ProfsTer9) n.599del n.674del | dbSNP |
| 15 | g.66435109A>C | CA392929211 | MAP2K1 | c.97A>C (p.Thr33Pro) c.163A>C (p.Thr55Pro) n.599A>C n.674A>C | |
| 15 | g.66435109A>G | CA392929213 | MAP2K1 | c.97A>G (p.Thr33Ala) c.163A>G (p.Thr55Ala) n.599A>G n.674A>G | |
| 15 | g.66435109A>T | CA392929215 | MAP2K1 | c.97A>T (p.Thr33Ser) c.163A>T (p.Thr55Ser) n.599A>T n.674A>T | |
| 15 | g.66435110C>A | CA392929216 | MAP2K1 | c.98C>A (p.Thr33Asn) c.164C>A (p.Thr55Asn) n.600C>A n.675C>A | dbSNP |
| 15 | g.66435110C>G | CA392929218 | MAP2K1 | c.98C>G (p.Thr33Ser) c.164C>G (p.Thr55Ser) n.600C>G n.675C>G | dbSNP |
| 15 | g.66435110C>T | CA392929220 | MAP2K1 | c.98C>T (p.Thr33Ile) c.164C>T (p.Thr55Ile) n.600C>T n.675C>T | dbSNP |
| 15 | g.66435112del | CA2731113721 | MAP2K1 | c.100del (p.Gln34ArgfsTer8) c.166del (p.Gln56ArgfsTer8) n.602del n.677del | dbSNP |
| 15 | g.66435111C>A | CA490855935 | MAP2K1 | c.99C>A (p.Thr33=) c.165C>A (p.Thr55=) n.601C>A n.676C>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.66435111C= | CA2184071741 | MAP2K1 | c.99C= (p.Thr33=) c.165C= (p.Thr55=) n.601C= n.676C= | |
| 15 | g.66435111C>G | CA7623878 | MAP2K1 | c.99C>G (p.Thr33=) c.165C>G (p.Thr55=) n.601C>G n.676C>G | dbSNP ExAC gnomAD v2 |
| 15 | g.66435111C>T | CA490855937 | MAP2K1 | c.99C>T (p.Thr33=) c.165C>T (p.Thr55=) n.601C>T n.676C>T | dbSNP gnomAD v4 |
| 15 | g.66435111_66435125del | CA912992484 | MAP2K1 | c.99_113del (p.Gln34_Val38del) c.165_179del (p.Gln56_Val60del) n.601_615del n.676_690del | ClinVar |
| 15 | g.66435112C>A | CA392929222 | MAP2K1 | c.100C>A (p.Gln34Lys) c.166C>A (p.Gln56Lys) n.602C>A n.677C>A | dbSNP |
| 15 | g.66435112C= | CA2184071742 | MAP2K1 | c.100C= (p.Gln34=) c.166C= (p.Gln56=) n.602C= n.677C= | |
| 15 | g.66435112C>G | CA392929224 | MAP2K1 | c.100C>G (p.Gln34Glu) c.166C>G (p.Gln56Glu) n.602C>G n.677C>G | dbSNP |
| 15 | g.66435112C>T | CA392929226 | MAP2K1 | c.100C>T (p.Gln34Ter) c.166C>T (p.Gln56Ter) n.602C>T n.677C>T | dbSNP gnomAD v4 |
| 15 | g.66435113A= | CA2184071743 | MAP2K1 | c.101A= (p.Gln34=) c.167A= (p.Gln56=) n.603A= n.678A= | |
| 15 | g.66435113A>C | CA16602453 | MAP2K1 | c.101A>C (p.Gln34Pro) c.167A>C (p.Gln56Pro) n.603A>C n.678A>C | ClinVar dbSNP |
| 15 | g.66435113A>G | CA392929230 | MAP2K1 | c.101A>G (p.Gln34Arg) c.167A>G (p.Gln56Arg) n.603A>G n.678A>G | dbSNP |
| 15 | g.66435113A>T | CA392929227 | MAP2K1 | c.101A>T (p.Gln34Leu) c.167A>T (p.Gln56Leu) n.603A>T n.678A>T | dbSNP |
| 15 | g.66435113_66435127del | CA645570533 | MAP2K1 | c.101_115del (p.Gln34_Gly39delinsArg) c.167_181del (p.Gln56_Gly61delinsArg) n.603_617del n.678_692del | COSMIC |
| 15 | g.66435114G>A | CA490855939 | MAP2K1 | c.102G>A (p.Gln34=) c.168G>A (p.Gln56=) n.604G>A n.679G>A | dbSNP |
| 15 | g.66435114G>C | CA392929232 | MAP2K1 | c.102G>C (p.Gln34His) c.168G>C (p.Gln56His) n.604G>C n.679G>C | dbSNP |
| 15 | g.66435114G>T | CA392929234 | MAP2K1 | c.102G>T (p.Gln34His) c.168G>T (p.Gln56His) n.604G>T n.679G>T | |
| 15 | g.66435114_66435128del | CA645570535 | MAP2K1 | c.102_116del (p.Lys35_Gly39del) c.168_182del (p.Lys57_Gly61del) n.604_618del n.679_693del | COSMIC |