WARNING - Protein Allele ID and Protein Sequence HGVS API Requests Temporarily Disabled:
We are investigating the periodic unresponsiveness in the Registry.
Although replication attempts were unsuccessful, there is a high correlation with protein alleles. And with haplotype HGVS queries.
This temporarily affects the API and the UI.
We are investigating the periodic unresponsiveness in the Registry.
Although replication attempts were unsuccessful, there is a high correlation with protein alleles. And with haplotype HGVS queries.
This temporarily affects the API and the UI.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 9 | g.35065351C>A | CA373289525 | VCP | c.476G>T (p.Arg159Leu) c.341G>T (p.Arg114Leu) n.748G>T n.822G>T c.470G>T (p.Arg157Leu) c.*447G>T (n.*447G>T) n.746G>T n.797G>T c.31G>T c.198G>T (p.Ala66=) c.228G>T c.642G>T n.672G>T | |
| 9 | g.35065351C= | CA1845842438 | VCP | c.476G= (p.Arg159=) c.341G= (p.Arg114=) n.748G= n.822G= c.470G= (p.Arg157=) c.*447G= (n.*447G=) n.746G= n.797G= c.31G= c.198G= (p.Ala66=) c.228G= c.642G= n.672G= | |
| 9 | g.35065351C>G | CA373289519 | VCP | c.476G>C (p.Arg159Pro) c.341G>C (p.Arg114Pro) n.748G>C n.822G>C c.470G>C (p.Arg157Pro) c.*447G>C (n.*447G>C) n.746G>C n.797G>C c.31G>C c.198G>C (p.Ala66=) c.228G>C c.642G>C n.672G>C | |
| 9 | g.35065351C>T | CA254408 | VCP | c.476G>A (p.Arg159His) c.341G>A (p.Arg114His) n.748G>A n.822G>A c.470G>A (p.Arg157His) c.*447G>A (n.*447G>A) n.746G>A n.797G>A c.31G>A c.198G>A (p.Ala66=) c.228G>A c.642G>A n.672G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 9 | g.35065352G>A | CA5039453 | VCP | c.475C>T (p.Arg159Cys) c.340C>T (p.Arg114Cys) n.747C>T n.821C>T c.469C>T (p.Arg157Cys) c.*446C>T (n.*446C>T) n.745C>T n.796C>T c.30C>T c.197C>T (p.Ala66Val) c.227C>T c.641C>T n.671C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 9 | g.35065352G>C | CA259748 | VCP | c.475C>G (p.Arg159Gly) c.340C>G (p.Arg114Gly) n.747C>G n.821C>G c.469C>G (p.Arg157Gly) c.*446C>G (n.*446C>G) n.745C>G n.796C>G c.30C>G c.197C>G (p.Ala66Gly) c.227C>G c.641C>G n.671C>G | ClinVar dbSNP |
| 9 | g.35065352G= | CA1845842447 | VCP | c.475C= (p.Arg159=) c.340C= (p.Arg114=) n.747C= n.821C= c.469C= (p.Arg157=) c.*446C= (n.*446C=) n.745C= n.796C= c.30C= c.197C= (p.Ala66=) c.227C= c.641C= n.671C= | |
| 9 | g.35065352G>T | CA373289529 | VCP | c.475C>A (p.Arg159Ser) c.340C>A (p.Arg114Ser) n.747C>A n.821C>A c.469C>A (p.Arg157Ser) c.*446C>A (n.*446C>A) n.745C>A n.796C>A c.30C>A c.197C>A (p.Ala66Glu) c.227C>A c.641C>A n.671C>A | ClinVar dbSNP |
| 9 | g.35065353C>A | CA373289533 | VCP | c.474G>T (p.Met158Ile) c.339G>T (p.Met113Ile) n.746G>T n.820G>T c.468G>T (p.Met156Ile) c.*445G>T (n.*445G>T) n.744G>T n.795G>T c.29G>T c.196G>T (p.Ala66Ser) c.226G>T c.640G>T n.670G>T | |
| 9 | g.35065353C>G | CA373289541 | VCP | c.474G>C (p.Met158Ile) c.339G>C (p.Met113Ile) n.746G>C n.820G>C c.468G>C (p.Met156Ile) c.*445G>C (n.*445G>C) n.744G>C n.795G>C c.29G>C c.196G>C (p.Ala66Pro) c.226G>C c.640G>C n.670G>C | |
| 9 | g.35065353C>T | CA373289555 | VCP | c.474G>A (p.Met158Ile) c.339G>A (p.Met113Ile) n.746G>A n.820G>A c.468G>A (p.Met156Ile) c.*445G>A (n.*445G>A) n.744G>A n.795G>A c.29G>A c.196G>A (p.Ala66Thr) c.226G>A c.640G>A n.670G>A | |
| 9 | g.35065354A= | CA1845842456 | VCP | c.473T= (p.Met158=) c.338T= (p.Met113=) n.745T= n.819T= c.467T= (p.Met156=) c.*444T= (n.*444T=) n.743T= n.794T= c.28T= c.195T= (p.Asp65=) c.225T= c.639T= n.669T= | |
| 9 | g.35065354A>C | CA373289559 | VCP | c.473T>G (p.Met158Arg) c.338T>G (p.Met113Arg) n.745T>G n.819T>G c.467T>G (p.Met156Arg) c.*444T>G (n.*444T>G) n.743T>G n.794T>G c.28T>G c.195T>G (p.Asp65Glu) c.225T>G c.639T>G n.669T>G | |
| 9 | g.35065354A>G | CA373289561 | VCP | c.473T>C (p.Met158Thr) c.338T>C (p.Met113Thr) n.745T>C n.819T>C c.467T>C (p.Met156Thr) c.*444T>C (n.*444T>C) n.743T>C n.794T>C c.28T>C c.195T>C (p.Asp65=) c.225T>C c.639T>C n.669T>C | dbSNP |
| 9 | g.35065354A>T | CA373289560 | VCP | c.473T>A (p.Met158Lys) c.338T>A (p.Met113Lys) n.745T>A n.819T>A c.467T>A (p.Met156Lys) c.*444T>A (n.*444T>A) n.743T>A n.794T>A c.28T>A c.195T>A (p.Asp65Glu) c.225T>A c.639T>A n.669T>A | |
| 9 | g.35065355T>A | CA373289568 | VCP | c.472A>T (p.Met158Leu) c.337A>T (p.Met113Leu) n.744A>T n.818A>T c.466A>T (p.Met156Leu) c.*443A>T (n.*443A>T) n.742A>T n.793A>T c.27A>T c.194A>T (p.Asp65Val) c.224A>T c.638A>T n.668A>T | |
| 9 | g.35065355T>C | CA373289580 | VCP | c.472A>G (p.Met158Val) c.337A>G (p.Met113Val) n.744A>G n.818A>G c.466A>G (p.Met156Val) c.*443A>G (n.*443A>G) n.742A>G n.793A>G c.27A>G c.194A>G (p.Asp65Gly) c.224A>G c.638A>G n.668A>G | ClinVar dbSNP |
| 9 | g.35065355T>G | CA373289585 | VCP | c.472A>C (p.Met158Leu) c.337A>C (p.Met113Leu) n.744A>C n.818A>C c.466A>C (p.Met156Leu) c.*443A>C (n.*443A>C) n.742A>C n.793A>C c.27A>C c.194A>C (p.Asp65Ala) c.224A>C c.638A>C n.668A>C | |
| 9 | g.35065355T= | CA1845842462 | VCP | c.472A= (p.Met158=) c.337A= (p.Met113=) n.744A= n.818A= c.466A= (p.Met156=) c.*443A= (n.*443A=) n.742A= n.793A= c.27A= c.194A= (p.Asp65=) c.224A= c.638A= n.668A= | |
| 9 | g.35065356C>A | CA464410432 | VCP | c.471G>T (p.Gly157=) c.336G>T (p.Gly112=) n.743G>T n.817G>T c.465G>T (p.Gly155=) c.*442G>T (n.*442G>T) n.741G>T n.792G>T c.26G>T c.193G>T (p.Asp65Tyr) c.223G>T c.637G>T n.667G>T | |
| 9 | g.35065356C= | CA1845842468 | VCP | c.471G= (p.Gly157=) c.336G= (p.Gly112=) n.743G= n.817G= c.465G= (p.Gly155=) c.*442G= (n.*442G=) n.741G= n.792G= c.26G= c.193G= (p.Asp65=) c.223G= c.637G= n.667G= | |
| 9 | g.35065356C>G | CA464410434 | VCP | c.471G>C (p.Gly157=) c.336G>C (p.Gly112=) n.743G>C n.817G>C c.465G>C (p.Gly155=) c.*442G>C (n.*442G>C) n.741G>C n.792G>C c.26G>C c.193G>C (p.Asp65His) c.223G>C c.637G>C n.667G>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.35065356C>T | CA464410438 | VCP | c.471G>A (p.Gly157=) c.336G>A (p.Gly112=) n.743G>A n.817G>A c.465G>A (p.Gly155=) c.*442G>A (n.*442G>A) n.741G>A n.792G>A c.26G>A c.193G>A (p.Asp65Asn) c.223G>A c.637G>A n.667G>A | |
| 9 | g.35065357C>A | CA373289590 | VCP | c.470G>T (p.Gly157Val) c.335G>T (p.Gly112Val) n.742G>T n.816G>T c.464G>T (p.Gly155Val) c.*441G>T (n.*441G>T) n.740G>T n.791G>T c.25G>T c.192G>T (p.Trp64Cys) c.222G>T c.636G>T n.666G>T | |
| 9 | g.35065357C>G | CA373289591 | VCP | c.470G>C (p.Gly157Ala) c.335G>C (p.Gly112Ala) n.742G>C n.816G>C c.464G>C (p.Gly155Ala) c.*441G>C (n.*441G>C) n.740G>C n.791G>C c.25G>C c.192G>C (p.Trp64Cys) c.222G>C c.636G>C n.666G>C | |
| 9 | g.35065357C>T | CA373289592 | VCP | c.470G>A (p.Gly157Glu) c.335G>A (p.Gly112Glu) n.742G>A n.816G>A c.464G>A (p.Gly155Glu) c.*441G>A (n.*441G>A) n.740G>A n.791G>A c.25G>A c.192G>A (p.Trp64Ter) c.222G>A c.636G>A n.666G>A | |
| 9 | g.35065358C>A | CA373289594 | VCP | c.469G>T (p.Gly157Trp) c.334G>T (p.Gly112Trp) n.741G>T n.815G>T c.463G>T (p.Gly155Trp) c.*440G>T (n.*440G>T) n.739G>T n.790G>T c.24G>T c.191G>T (p.Trp64Leu) c.221G>T c.635G>T n.665G>T | dbSNP |
| 9 | g.35065358C= | CA1845842478 | VCP | c.469G= (p.Gly157=) c.334G= (p.Gly112=) n.741G= n.815G= c.463G= (p.Gly155=) c.*440G= (n.*440G=) n.739G= n.790G= c.24G= c.191G= (p.Trp64=) c.221G= c.635G= n.665G= | |
| 9 | g.35065358C>G | CA373289597 | VCP | c.469G>C (p.Gly157Arg) c.334G>C (p.Gly112Arg) n.741G>C n.815G>C c.463G>C (p.Gly155Arg) c.*440G>C (n.*440G>C) n.739G>C n.790G>C c.24G>C c.191G>C (p.Trp64Ser) c.221G>C c.635G>C n.665G>C | ClinVar dbSNP |
| 9 | g.35065358C>T | CA373289608 | VCP | c.469G>A (p.Gly157Arg) c.334G>A (p.Gly112Arg) n.741G>A n.815G>A c.463G>A (p.Gly155Arg) c.*440G>A (n.*440G>A) n.739G>A n.790G>A c.24G>A c.191G>A (p.Trp64Ter) c.221G>A c.635G>A n.665G>A | ClinVar dbSNP |
| 9 | g.35065359A>C | CA464410446 | VCP | c.468T>G (p.Gly156=) c.333T>G (p.Gly111=) n.740T>G n.814T>G c.462T>G (p.Gly154=) c.*439T>G (n.*439T>G) n.738T>G n.789T>G c.23T>G c.190T>G (p.Trp64Gly) c.220T>G c.634T>G n.664T>G | |
| 9 | g.35065359A>G | CA464410449 | VCP | c.468T>C (p.Gly156=) c.333T>C (p.Gly111=) n.740T>C n.814T>C c.462T>C (p.Gly154=) c.*439T>C (n.*439T>C) n.738T>C n.789T>C c.23T>C c.190T>C (p.Trp64Arg) c.220T>C c.634T>C n.664T>C | |
| 9 | g.35065359A>T | CA464410462 | VCP | c.468T>A (p.Gly156=) c.333T>A (p.Gly111=) n.740T>A n.814T>A c.462T>A (p.Gly154=) c.*439T>A (n.*439T>A) n.738T>A n.789T>A c.23T>A c.190T>A (p.Trp64Arg) c.220T>A c.634T>A n.664T>A | |
| 9 | g.35065360C>A | CA373289611 | VCP | c.467G>T (p.Gly156Val) c.332G>T (p.Gly111Val) n.739G>T n.813G>T c.461G>T (p.Gly154Val) c.*438G>T (n.*438G>T) n.737G>T n.788G>T c.22G>T c.189G>T (p.Trp63Cys) c.219G>T c.633G>T n.663G>T | ClinVar |
| 9 | g.35065360C>G | CA373289613 | VCP | c.467G>C (p.Gly156Ala) c.332G>C (p.Gly111Ala) n.739G>C n.813G>C c.461G>C (p.Gly154Ala) c.*438G>C (n.*438G>C) n.737G>C n.788G>C c.22G>C c.189G>C (p.Trp63Cys) c.219G>C c.633G>C n.663G>C | |
| 9 | g.35065360C>T | CA373289616 | VCP | c.467G>A (p.Gly156Asp) c.332G>A (p.Gly111Asp) n.739G>A n.813G>A c.461G>A (p.Gly154Asp) c.*438G>A (n.*438G>A) n.737G>A n.788G>A c.22G>A c.189G>A (p.Trp63Ter) c.219G>A c.633G>A n.663G>A | |
| 9 | g.35065361C>A | CA373289621 | VCP | c.466G>T (p.Gly156Cys) c.331G>T (p.Gly111Cys) n.738G>T n.812G>T c.460G>T (p.Gly154Cys) c.*437G>T (n.*437G>T) n.736G>T n.787G>T c.21G>T c.188G>T (p.Trp63Leu) c.218G>T c.632G>T n.662G>T | |
| 9 | g.35065361C= | CA1845842484 | VCP | c.466G= (p.Gly156=) c.331G= (p.Gly111=) n.738G= n.812G= c.460G= (p.Gly154=) c.*437G= (n.*437G=) n.736G= n.787G= c.21G= c.188G= (p.Trp63=) c.218G= c.632G= n.662G= | |
| 9 | g.35065361C>G | CA373289626 | VCP | c.466G>C (p.Gly156Arg) c.331G>C (p.Gly111Arg) n.738G>C n.812G>C c.460G>C (p.Gly154Arg) c.*437G>C (n.*437G>C) n.736G>C n.787G>C c.21G>C c.188G>C (p.Trp63Ser) c.218G>C c.632G>C n.662G>C | |
| 9 | g.35065361C>T | CA373289624 | VCP | c.466G>A (p.Gly156Ser) c.331G>A (p.Gly111Ser) n.738G>A n.812G>A c.460G>A (p.Gly154Ser) c.*437G>A (n.*437G>A) n.736G>A n.787G>A c.21G>A c.188G>A (p.Trp63Ter) c.218G>A c.632G>A n.662G>A | ClinVar dbSNP |
| 9 | g.35065362A= | CA1845842488 | VCP | c.465T= (p.Arg155=) c.330T= (p.Arg110=) n.737T= n.811T= c.459T= (p.Arg153=) c.*436T= (n.*436T=) n.735T= n.786T= c.20T= c.187T= (p.Trp63=) c.217T= c.631T= n.661T= | |
| 9 | g.35065362A>C | CA5039454 | VCP | c.465T>G (p.Arg155=) c.330T>G (p.Arg110=) n.737T>G n.811T>G c.459T>G (p.Arg153=) c.*436T>G (n.*436T>G) n.735T>G n.786T>G c.20T>G c.187T>G (p.Trp63Gly) c.217T>G c.631T>G n.661T>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.35065362A>G | CA464410468 | VCP | c.465T>C (p.Arg155=) c.330T>C (p.Arg110=) n.737T>C n.811T>C c.459T>C (p.Arg153=) c.*436T>C (n.*436T>C) n.735T>C n.786T>C c.20T>C c.187T>C (p.Trp63Arg) c.217T>C c.631T>C n.661T>C | dbSNP gnomAD v4 |
| 9 | g.35065362A>T | CA464410472 | VCP | c.465T>A (p.Arg155=) c.330T>A (p.Arg110=) n.737T>A n.811T>A c.459T>A (p.Arg153=) c.*436T>A (n.*436T>A) n.735T>A n.786T>A c.20T>A c.187T>A (p.Trp63Arg) c.217T>A c.631T>A n.661T>A | |
| 9 | g.35065363C>A | CA373289634 | VCP | c.464G>T (p.Arg155Leu) c.329G>T (p.Arg110Leu) n.736G>T n.810G>T c.458G>T (p.Arg153Leu) c.*435G>T (n.*435G>T) n.734G>T n.785G>T c.19G>T c.186G>T (p.Pro62=) c.216G>T c.630G>T n.660G>T | dbSNP |
| 9 | g.35065363C= | CA1845842492 | VCP | c.464G= (p.Arg155=) c.329G= (p.Arg110=) n.736G= n.810G= c.458G= (p.Arg153=) c.*435G= (n.*435G=) n.734G= n.785G= c.19G= c.186G= (p.Pro62=) c.216G= c.630G= n.660G= | |
| 9 | g.35065363C>G | CA254404 | VCP | c.464G>C (p.Arg155Pro) c.329G>C (p.Arg110Pro) n.736G>C n.810G>C c.458G>C (p.Arg153Pro) c.*435G>C (n.*435G>C) n.734G>C n.785G>C c.19G>C c.186G>C (p.Pro62=) c.216G>C c.630G>C n.660G>C | ClinVar dbSNP |
| 9 | g.35065363C>T | CA128983 | VCP | c.464G>A (p.Arg155His) c.329G>A (p.Arg110His) n.736G>A n.810G>A c.458G>A (p.Arg153His) c.*435G>A (n.*435G>A) n.734G>A n.785G>A c.19G>A c.186G>A (p.Pro62=) c.216G>A c.630G>A n.660G>A | ClinVar dbSNP gnomAD v4 |
| 9 | g.35065364G>A | CA254398 | VCP | c.463C>T (p.Arg155Cys) c.328C>T (p.Arg110Cys) n.735C>T n.809C>T c.457C>T (p.Arg153Cys) c.*434C>T (n.*434C>T) n.733C>T n.784C>T c.18C>T c.185C>T (p.Pro62Leu) c.215C>T c.629C>T n.659C>T | ClinVar dbSNP COSMIC |
| 9 | g.35065364G>C | CA277489 | VCP | c.463C>G (p.Arg155Gly) c.328C>G (p.Arg110Gly) n.735C>G n.809C>G c.457C>G (p.Arg153Gly) c.*434C>G (n.*434C>G) n.733C>G n.784C>G c.18C>G c.185C>G (p.Pro62Arg) c.215C>G c.629C>G n.659C>G | ClinVar dbSNP |