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.74089213C>A | CA377272256 | VCL | c.1040C>A (p.Pro347Gln) c.56C>A (p.Pro19Gln) n.332-11841C>A n.3843C>A c.*795C>A (n.*795C>A) c.1043C>A (p.Pro348Gln) n.89+719G>T | ClinVar dbSNP gnomAD v4 |
| 10 | g.74089213C= | CA1919902958 | VCL | c.1040C= (p.Pro347=) c.56C= (p.Pro19=) n.332-11841C= n.3843C= c.*795C= (n.*795C=) c.1043C= (p.Pro348=) n.89+719G= | |
| 10 | g.74089213C>G | CA377272258 | VCL | c.1040C>G (p.Pro347Arg) c.56C>G (p.Pro19Arg) n.332-11841C>G n.3843C>G c.*795C>G (n.*795C>G) c.1043C>G (p.Pro348Arg) n.89+719G>C | |
| 10 | g.74089213C>T | CA5562919 | VCL | c.1040C>T (p.Pro347Leu) c.56C>T (p.Pro19Leu) n.332-11841C>T n.3843C>T c.*795C>T (n.*795C>T) c.1043C>T (p.Pro348Leu) n.89+719G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.74089214G>A | CA5562921 | VCL | c.1041G>A (p.Pro347=) c.57G>A (p.Pro19=) n.332-11840G>A n.3844G>A c.*796G>A (n.*796G>A) c.1044G>A (p.Pro348=) n.89+718C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
| 10 | g.74089214G>C | CA5562920 | VCL | c.1041G>C (p.Pro347=) c.57G>C (p.Pro19=) n.332-11840G>C n.3844G>C c.*796G>C (n.*796G>C) c.1044G>C (p.Pro348=) n.89+718C>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.74089214G= | CA1919902959 | VCL | c.1041G= (p.Pro347=) c.57G= (p.Pro19=) n.332-11840G= n.3844G= c.*796G= (n.*796G=) c.1044G= (p.Pro348=) n.89+718C= | |
| 10 | g.74089214G>T | CA470172284 | VCL | c.1041G>T (p.Pro347=) c.57G>T (p.Pro19=) n.332-11840G>T n.3844G>T c.*796G>T (n.*796G>T) c.1044G>T (p.Pro348=) n.89+718C>A | |
| 10 | g.74089215G>A | CA377272266 | VCL | c.1042G>A (p.Val348Met) c.58G>A (p.Val20Met) n.332-11839G>A n.3845G>A c.*797G>A (n.*797G>A) c.1045G>A (p.Val349Met) n.89+717C>T | ClinVar dbSNP |
| 10 | g.74089215G>C | CA377272268 | VCL | c.1042G>C (p.Val348Leu) c.58G>C (p.Val20Leu) n.332-11839G>C n.3845G>C c.*797G>C (n.*797G>C) c.1045G>C (p.Val349Leu) n.89+717C>G | |
| 10 | g.74089215G>T | CA377272272 | VCL | c.1042G>T (p.Val348Leu) c.58G>T (p.Val20Leu) n.332-11839G>T n.3845G>T c.*797G>T (n.*797G>T) c.1045G>T (p.Val349Leu) n.89+717C>A | |
| 10 | g.74089216T>A | CA377272273 | VCL | c.1043T>A (p.Val348Glu) c.59T>A (p.Val20Glu) n.332-11838T>A n.3846T>A c.*798T>A (n.*798T>A) c.1046T>A (p.Val349Glu) n.89+716A>T | |
| 10 | g.74089216T>C | CA377272276 | VCL | c.1043T>C (p.Val348Ala) c.59T>C (p.Val20Ala) n.332-11838T>C n.3846T>C c.*798T>C (n.*798T>C) c.1046T>C (p.Val349Ala) n.89+716A>G | |
| 10 | g.74089216T>G | CA377272278 | VCL | c.1043T>G (p.Val348Gly) c.59T>G (p.Val20Gly) n.332-11838T>G n.3846T>G c.*798T>G (n.*798T>G) c.1046T>G (p.Val349Gly) n.89+716A>C | |
| 10 | g.74089217G>A | CA470172285 | VCL | c.1044G>A (p.Val348=) c.60G>A (p.Val20=) n.332-11837G>A n.3847G>A c.*799G>A (n.*799G>A) c.1047G>A (p.Val349=) n.89+715C>T | gnomAD v4 |
| 10 | g.74089217G>C | CA470172286 | VCL | c.1044G>C (p.Val348=) c.60G>C (p.Val20=) n.332-11837G>C n.3847G>C c.*799G>C (n.*799G>C) c.1047G>C (p.Val349=) n.89+715C>G | |
| 10 | g.74089217G>T | CA470172287 | VCL | c.1044G>T (p.Val348=) c.60G>T (p.Val20=) n.332-11837G>T n.3847G>T c.*799G>T (n.*799G>T) c.1047G>T (p.Val349=) n.89+715C>A | |
| 10 | g.74089218G>A | CA5562922 | VCL | c.1045G>A (p.Ala349Thr) c.61G>A (p.Ala21Thr) n.332-11836G>A n.3848G>A c.*800G>A (n.*800G>A) c.1048G>A (p.Ala350Thr) n.89+714C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 10 | g.74089218G>C | CA377272284 | VCL | c.1045G>C (p.Ala349Pro) c.61G>C (p.Ala21Pro) n.332-11836G>C n.3848G>C c.*800G>C (n.*800G>C) c.1048G>C (p.Ala350Pro) n.89+714C>G | |
| 10 | g.74089218G= | CA1919902960 | VCL | c.1045G= (p.Ala349=) c.61G= (p.Ala21=) n.332-11836G= n.3848G= c.*800G= (n.*800G=) c.1048G= (p.Ala350=) n.89+714C= | |
| 10 | g.74089218G>T | CA377272282 | VCL | c.1045G>T (p.Ala349Ser) c.61G>T (p.Ala21Ser) n.332-11836G>T n.3848G>T c.*800G>T (n.*800G>T) c.1048G>T (p.Ala350Ser) n.89+714C>A | |
| 10 | g.74089219C>A | CA377272287 | VCL | c.1046C>A (p.Ala349Asp) c.62C>A (p.Ala21Asp) n.332-11835C>A n.3849C>A c.*801C>A (n.*801C>A) c.1049C>A (p.Ala350Asp) n.89+713G>T | |
| 10 | g.74089219C= | CA1919902961 | VCL | c.1046C= (p.Ala349=) c.62C= (p.Ala21=) n.332-11835C= n.3849C= c.*801C= (n.*801C=) c.1049C= (p.Ala350=) n.89+713G= | |
| 10 | g.74089219C>G | CA377272288 | VCL | c.1046C>G (p.Ala349Gly) c.62C>G (p.Ala21Gly) n.332-11835C>G n.3849C>G c.*801C>G (n.*801C>G) c.1049C>G (p.Ala350Gly) n.89+713G>C | |
| 10 | g.74089219C>T | CA5562923 | VCL | c.1046C>T (p.Ala349Val) c.62C>T (p.Ala21Val) n.332-11835C>T n.3849C>T c.*801C>T (n.*801C>T) c.1049C>T (p.Ala350Val) n.89+713G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.74089220C>A | CA470172291 | VCL | c.1047C>A (p.Ala349=) c.63C>A (p.Ala21=) n.332-11834C>A n.3850C>A c.*802C>A (n.*802C>A) c.1050C>A (p.Ala350=) n.89+712G>T | gnomAD v4 |
| 10 | g.74089220C>G | CA470172293 | VCL | c.1047C>G (p.Ala349=) c.63C>G (p.Ala21=) n.332-11834C>G n.3850C>G c.*802C>G (n.*802C>G) c.1050C>G (p.Ala350=) n.89+712G>C | |
| 10 | g.74089220C>T | CA470172292 | VCL | c.1047C>T (p.Ala349=) c.63C>T (p.Ala21=) n.332-11834C>T n.3850C>T c.*802C>T (n.*802C>T) c.1050C>T (p.Ala350=) n.89+712G>A | ClinVar |
| 10 | g.74089221A= | CA1919902962 | VCL | c.1048A= (p.Met350=) c.64A= (p.Met22=) n.332-11833A= n.3851A= c.*803A= (n.*803A=) c.1051A= (p.Met351=) n.89+711T= | |
| 10 | g.74089221A>C | CA377272289 | VCL | c.1048A>C (p.Met350Leu) c.64A>C (p.Met22Leu) n.332-11833A>C n.3851A>C c.*803A>C (n.*803A>C) c.1051A>C (p.Met351Leu) n.89+711T>G | dbSNP gnomAD v4 |
| 10 | g.74089221A>G | CA377272290 | VCL | c.1048A>G (p.Met350Val) c.64A>G (p.Met22Val) n.332-11833A>G n.3851A>G c.*803A>G (n.*803A>G) c.1051A>G (p.Met351Val) n.89+711T>C | |
| 10 | g.74089221A>T | CA377272291 | VCL | c.1048A>T (p.Met350Leu) c.64A>T (p.Met22Leu) n.332-11833A>T n.3851A>T c.*803A>T (n.*803A>T) c.1051A>T (p.Met351Leu) n.89+711T>A | |
| 10 | g.74089222T>A | CA377272292 | VCL | c.1049T>A (p.Met350Lys) c.65T>A (p.Met22Lys) n.332-11832T>A n.3852T>A c.*804T>A (n.*804T>A) c.1052T>A (p.Met351Lys) n.89+710A>T | |
| 10 | g.74089222T>C | CA5562924 | VCL | c.1049T>C (p.Met350Thr) c.65T>C (p.Met22Thr) n.332-11832T>C n.3852T>C c.*804T>C (n.*804T>C) c.1052T>C (p.Met351Thr) n.89+710A>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 10 | g.74089222T>G | CA377272294 | VCL | c.1049T>G (p.Met350Arg) c.65T>G (p.Met22Arg) n.332-11832T>G n.3852T>G c.*804T>G (n.*804T>G) c.1052T>G (p.Met351Arg) n.89+710A>C | |
| 10 | g.74089222T= | CA1919902963 | VCL | c.1049T= (p.Met350=) c.65T= (p.Met22=) n.332-11832T= n.3852T= c.*804T= (n.*804T=) c.1052T= (p.Met351=) n.89+710A= | |
| 10 | g.74089223G>A | CA5562925 | VCL | c.1050G>A (p.Met350Ile) c.66G>A (p.Met22Ile) n.332-11831G>A n.3853G>A c.*805G>A (n.*805G>A) c.1053G>A (p.Met351Ile) n.89+709C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.74089223G>C | CA377272297 | VCL | c.1050G>C (p.Met350Ile) c.66G>C (p.Met22Ile) n.332-11831G>C n.3853G>C c.*805G>C (n.*805G>C) c.1053G>C (p.Met351Ile) n.89+709C>G | |
| 10 | g.74089223G= | CA1919902964 | VCL | c.1050G= (p.Met350=) c.66G= (p.Met22=) n.332-11831G= n.3853G= c.*805G= (n.*805G=) c.1053G= (p.Met351=) n.89+709C= | |
| 10 | g.74089223G>T | CA377272298 | VCL | c.1050G>T (p.Met350Ile) c.66G>T (p.Met22Ile) n.332-11831G>T n.3853G>T c.*805G>T (n.*805G>T) c.1053G>T (p.Met351Ile) n.89+709C>A | |
| 10 | g.74089224C>A | CA377272306 | VCL | c.1051C>A (p.Gln351Lys) c.67C>A (p.Gln23Lys) n.332-11830C>A n.3854C>A c.*806C>A (n.*806C>A) c.1054C>A (p.Gln352Lys) n.89+708G>T | |
| 10 | g.74089224C= | CA1919902965 | VCL | c.1051C= (p.Gln351=) c.67C= (p.Gln23=) n.332-11830C= n.3854C= c.*806C= (n.*806C=) c.1054C= (p.Gln352=) n.89+708G= | |
| 10 | g.74089224C>G | CA377272308 | VCL | c.1051C>G (p.Gln351Glu) c.67C>G (p.Gln23Glu) n.332-11830C>G n.3854C>G c.*806C>G (n.*806C>G) c.1054C>G (p.Gln352Glu) n.89+708G>C | |
| 10 | g.74089224C>T | CA377272301 | VCL | c.1051C>T (p.Gln351Ter) c.67C>T (p.Gln23Ter) n.332-11830C>T n.3854C>T c.*806C>T (n.*806C>T) c.1054C>T (p.Gln352Ter) n.89+708G>A | dbSNP |
| 10 | g.74089225A>C | CA377272311 | VCL | c.1052A>C (p.Gln351Pro) c.68A>C (p.Gln23Pro) n.332-11829A>C n.3855A>C c.*807A>C (n.*807A>C) c.1055A>C (p.Gln352Pro) n.89+707T>G | |
| 10 | g.74089225A>G | CA377272312 | VCL | c.1052A>G (p.Gln351Arg) c.68A>G (p.Gln23Arg) n.332-11829A>G n.3855A>G c.*807A>G (n.*807A>G) c.1055A>G (p.Gln352Arg) n.89+707T>C | |
| 10 | g.74089225A>T | CA377272315 | VCL | c.1052A>T (p.Gln351Leu) c.68A>T (p.Gln23Leu) n.332-11829A>T n.3855A>T c.*807A>T (n.*807A>T) c.1055A>T (p.Gln352Leu) n.89+707T>A | |
| 10 | g.74089226G>A | CA470172301 | VCL | c.1053G>A (p.Gln351=) c.69G>A (p.Gln23=) n.332-11828G>A n.3856G>A c.*808G>A (n.*808G>A) c.1056G>A (p.Gln352=) n.89+706C>T | |
| 10 | g.74089226G>C | CA377272318 | VCL | c.1053G>C (p.Gln351His) c.69G>C (p.Gln23His) n.332-11828G>C n.3856G>C c.*808G>C (n.*808G>C) c.1056G>C (p.Gln352His) n.89+706C>G | |
| 10 | g.74089226G>T | CA377272322 | VCL | c.1053G>T (p.Gln351His) c.69G>T (p.Gln23His) n.332-11828G>T n.3856G>T c.*808G>T (n.*808G>T) c.1056G>T (p.Gln352His) n.89+706C>A |