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 |
|---|---|---|---|---|---|
| 15 | g.48441698C>T | CA2628334327 | FBN1 | c.6163+23G>A (n.6163+23G>A) c.1162+23G>A (n.1162+23G>A) c.*1926+23G>A (n.*1926+23G>A) c.1470+23G>A n.283+23G>A | gnomAD v4 |
| 15 | g.48441702del | CA2628334328 | FBN1 | c.6163+21del (n.6163+21del) c.1162+21del (n.1162+21del) c.*1926+21del (n.*1926+21del) c.1470+21del n.283+21del | gnomAD v4 |
| 15 | g.48441703G>A | CA713401145 | FBN1 | c.6163+18C>T (n.6163+18C>T) c.1162+18C>T (n.1162+18C>T) c.*1926+18C>T (n.*1926+18C>T) c.1470+18C>T n.283+18C>T | dbSNP |
| 15 | g.48441703G>C | CA617836489 | FBN1 | c.6163+18C>G (n.6163+18C>G) c.1162+18C>G (n.1162+18C>G) c.*1926+18C>G (n.*1926+18C>G) c.1470+18C>G n.283+18C>G | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.48441703G= | CA2175508552 | FBN1 | c.6163+18C= (n.6163+18C=) c.1162+18C= (n.1162+18C=) c.*1926+18C= (n.*1926+18C=) c.1470+18C= n.283+18C= | |
| 15 | g.48441704C>A | CA713401160 | FBN1 | c.6163+17G>T (n.6163+17G>T) c.1162+17G>T (n.1162+17G>T) c.*1926+17G>T (n.*1926+17G>T) c.1470+17G>T n.283+17G>T | dbSNP |
| 15 | g.48441704C= | CA2175508556 | FBN1 | c.6163+17G= (n.6163+17G=) c.1162+17G= (n.1162+17G=) c.*1926+17G= (n.*1926+17G=) c.1470+17G= n.283+17G= | |
| 15 | g.48441704C>G | CA269530655 | FBN1 | c.6163+17G>C (n.6163+17G>C) c.1162+17G>C (n.1162+17G>C) c.*1926+17G>C (n.*1926+17G>C) c.1470+17G>C n.283+17G>C | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.48441709A>G | CA2628334336 | FBN1 | c.6163+12T>C (n.6163+12T>C) c.1162+12T>C (n.1162+12T>C) c.*1926+12T>C (n.*1926+12T>C) c.1470+12T>C n.283+12T>C | gnomAD v4 |
| 15 | g.48441710A= | CA2175508559 | FBN1 | c.6163+11T= (n.6163+11T=) c.1162+11T= (n.1162+11T=) c.*1926+11T= (n.*1926+11T=) c.1470+11T= n.283+11T= | |
| 15 | g.48441710A>C | CA713401161 | FBN1 | c.6163+11T>G (n.6163+11T>G) c.1162+11T>G (n.1162+11T>G) c.*1926+11T>G (n.*1926+11T>G) c.1470+11T>G n.283+11T>G | dbSNP |
| 15 | g.48441710A>G | CA914002823 | FBN1 | c.6163+11T>C (n.6163+11T>C) c.1162+11T>C (n.1162+11T>C) c.*1926+11T>C (n.*1926+11T>C) c.1470+11T>C n.283+11T>C | gnomAD v2 gnomAD v4 |
| 15 | g.48441712G>C | CA056343 | FBN1 | c.6163+9C>G (n.6163+9C>G) c.1162+9C>G (n.1162+9C>G) c.*1926+9C>G (n.*1926+9C>G) c.1470+9C>G n.283+9C>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.48441712G= | CA2175508561 | FBN1 | c.6163+9C= (n.6163+9C=) c.1162+9C= (n.1162+9C=) c.*1926+9C= (n.*1926+9C=) c.1470+9C= n.283+9C= | |
| 15 | g.48441712G>T | CA645584724 | FBN1 | c.6163+9C>A (n.6163+9C>A) c.1162+9C>A (n.1162+9C>A) c.*1926+9C>A (n.*1926+9C>A) c.1470+9C>A n.283+9C>A | dbSNP COSMIC |
| 15 | g.48441713A= | CA2175508565 | FBN1 | c.6163+8T= (n.6163+8T=) c.1162+8T= (n.1162+8T=) c.*1926+8T= (n.*1926+8T=) c.1470+8T= n.283+8T= | |
| 15 | g.48441713A>C | CA617836490 | FBN1 | c.6163+8T>G (n.6163+8T>G) c.1162+8T>G (n.1162+8T>G) c.*1926+8T>G (n.*1926+8T>G) c.1470+8T>G n.283+8T>G | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.48441715_48441720del | CA2695220184 | FBN1 | c.6163+3_6163+8del (n.6163+3_6163+8del) c.1162+3_1162+8del (n.1162+3_1162+8del) c.*1926+3_*1926+8del (n.*1926+3_*1926+8del) c.1470+3_1470+8del n.283+3_283+8del | |
| 15 | g.48441714C>T | CA2570387951 | FBN1 | c.6163+7G>A (n.6163+7G>A) c.1162+7G>A (n.1162+7G>A) c.*1926+7G>A (n.*1926+7G>A) c.1470+7G>A n.283+7G>A | |
| 15 | g.48441717_48441720del | CA2695220186 | FBN1 | c.6163+3_6163+6del (n.6163+3_6163+6del) c.1162+3_1162+6del (n.1162+3_1162+6del) c.*1926+3_*1926+6del (n.*1926+3_*1926+6del) c.1470+3_1470+6del n.283+3_283+6del | |
| 15 | g.48441717T>G | CA2499222977 | FBN1 | c.6163+4A>C (n.6163+4A>C) c.1162+4A>C (n.1162+4A>C) c.*1926+4A>C (n.*1926+4A>C) c.1470+4A>C n.283+4A>C | ClinVar dbSNP |
| 15 | g.48441718T= | CA2175508568 | FBN1 | c.6163+3A= (n.6163+3A=) c.1162+3A= (n.1162+3A=) c.*1926+3A= (n.*1926+3A=) c.1470+3A= n.283+3A= | |
| 15 | g.48441719A>C | CA392337846 | FBN1 | c.6163+2T>G (n.6163+2T>G) c.1162+2T>G (n.1162+2T>G) c.*1926+2T>G (n.*1926+2T>G) c.1470+2T>G n.283+2T>G | |
| 15 | g.48441719A>G | CA392337844 | FBN1 | c.6163+2T>C (n.6163+2T>C) c.1162+2T>C (n.1162+2T>C) c.*1926+2T>C (n.*1926+2T>C) c.1470+2T>C n.283+2T>C | |
| 15 | g.48441719A>T | CA392337845 | FBN1 | c.6163+2T>A (n.6163+2T>A) c.1162+2T>A (n.1162+2T>A) c.*1926+2T>A (n.*1926+2T>A) c.1470+2T>A n.283+2T>A | gnomAD v4 |
| 15 | g.48441719dup | CA304350 | FBN1 | c.6163+2dup (n.6163+2dup) c.1162+2dup (n.1162+2dup) c.*1926+2dup (n.*1926+2dup) c.1470+2dup n.283+2dup | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.48441719_48441720del | CA2740096627 | FBN1 | c.6163+1_6163+2del (n.6163+1_6163+2del) c.1162+1_1162+2del (n.1162+1_1162+2del) c.*1926+1_*1926+2del (n.*1926+1_*1926+2del) c.1470+1_1470+2del n.283+1_283+2del | ClinVar |
| 15 | g.48441724_48441731del | CA913203390 | FBN1 | c.6158_6163+2del c.1157_1162+2del c.*1921_*1926+2del c.1465_1470+2del n.278_283+2del | |
| 15 | g.48441720C>A | CA392337852 | FBN1 | c.6163+1G>T (n.6163+1G>T) c.1162+1G>T (n.1162+1G>T) c.*1926+1G>T (n.*1926+1G>T) c.1470+1G>T n.283+1G>T | |
| 15 | g.48441720C= | CA2175508579 | FBN1 | c.6163+1G= (n.6163+1G=) c.1162+1G= (n.1162+1G=) c.*1926+1G= (n.*1926+1G=) c.1470+1G= n.283+1G= | |
| 15 | g.48441720C>G | CA392337855 | FBN1 | c.6163+1G>C (n.6163+1G>C) c.1162+1G>C (n.1162+1G>C) c.*1926+1G>C (n.*1926+1G>C) c.1470+1G>C n.283+1G>C | |
| 15 | g.48441720C>T | CA392337857 | FBN1 | c.6163+1G>A (n.6163+1G>A) c.1162+1G>A (n.1162+1G>A) c.*1926+1G>A (n.*1926+1G>A) c.1470+1G>A n.283+1G>A | ClinVar dbSNP |
| 15 | g.48441721del | CA2695220188 | FBN1 | c.6163+1del c.1162+1del c.*1926+1del c.1470+1del n.283+1del | |
| 15 | g.48441720_48441846delinsCCTTGGCACCTTCTTCCACTGGAGGACAAGGAAAACCCTTCTGGACACAGACATTTGAAGCTGCCTTCAGTGTTACTGCATGTGCCCAGGGCACAAATTTCTGGCTCTTCGACACACTCATCAATAT | CA2175508586 | FBN1 | c.6038_6163+1delinsATATTGATGAGTGTGTCGAAGAGCCAGAAATTTGTGCCCTGGGCACATGCAGTAACACTGAAGGCAGCTTCAAATGTCTGTGTCCAGAAGGGTTTTCCTTGTCCTCCAGTGGAAGAAGGTGCCAAGG c.1037_1162+1delinsATATTGATGAGTGTGTCGAAGAGCCAGAAATTTGTGCCCTGGGCACATGCAGTAACACTGAAGGCAGCTTCAAATGTCTGTGTCCAGAAGGGTTTTCCTTGTCCTCCAGTGGAAGAAGGTGCCAAGG c.*1801_*1926+1delinsATATTGATGAGTGTGTCGAAGAGCCAGAAATTTGTGCCCTGGGCACATGCAGTAACACTGAAGGCAGCTTCAAATGTCTGTGTCCAGAAGGGTTTTCCTTGTCCTCCAGTGGAAGAAGGTGCCAAGG c.1345_1470+1delinsATATTGATGAGTGTGTCGAAGAGCCAGAAATTTGTGCCCTGGGCACATGCAGTAACACTGAAGGCAGCTTCAAATGTCTGTGTCCAGAAGGGTTTTCCTTGTCCTCCAGTGGAAGAAGGTGCCAAGG n.158_283+1delinsATATTGATGAGTGTGTCGAAGAGCCAGAAATTTGTGCCCTGGGCACATGCAGTAACACTGAAGGCAGCTTCAAATGTCTGTGTCCAGAAGGGTTTTCCTTGTCCTCCAGTGGAAGAAGGTGCCAAGG | |
| 15 | g.48441721C>A | CA392337862 | FBN1 | c.6163G>T (p.Asp2055Tyr) c.1162G>T (p.Asp388Tyr) c.*1926G>T (n.*1926G>T) c.1470G>T n.283G>T | |
| 15 | g.48441721C>G | CA392337865 | FBN1 | c.6163G>C (p.Asp2055His) c.1162G>C (p.Asp388His) c.*1926G>C (n.*1926G>C) c.1470G>C n.283G>C | |
| 15 | g.48441721C>T | CA392337867 | FBN1 | c.6163G>A (p.Asp2055Asn) c.1162G>A (p.Asp388Asn) c.*1926G>A (n.*1926G>A) c.1470G>A n.283G>A | |
| 15 | g.48441723_48441848del | CA658824940 | FBN1 | c.6038_6163del c.1037_1162del c.*1801_*1926del c.1345_1470del n.158_283del | ClinVar dbSNP |
| 15 | g.48441722T>A | CA392337869 | FBN1 | c.6162A>T (p.Gln2054His) c.1161A>T (p.Gln387His) c.*1925A>T (n.*1925A>T) c.1469A>T n.282A>T | |
| 15 | g.48441722T>C | CA490021242 | FBN1 | c.6162A>G (p.Gln2054=) c.1161A>G (p.Gln387=) c.*1925A>G (n.*1925A>G) c.1469A>G n.282A>G | ClinVar |
| 15 | g.48441722T>G | CA392337872 | FBN1 | c.6162A>C (p.Gln2054His) c.1161A>C (p.Gln387His) c.*1925A>C (n.*1925A>C) c.1469A>C n.282A>C | |
| 15 | g.48441723T>A | CA392337876 | FBN1 | c.6161A>T (p.Gln2054Leu) c.1160A>T (p.Gln387Leu) c.*1924A>T (n.*1924A>T) c.1468A>T n.281A>T | |
| 15 | g.48441723T>C | CA392337877 | FBN1 | c.6161A>G (p.Gln2054Arg) c.1160A>G (p.Gln387Arg) c.*1924A>G (n.*1924A>G) c.1468A>G n.281A>G | ClinVar dbSNP gnomAD v4 |
| 15 | g.48441723T>G | CA392337881 | FBN1 | c.6161A>C (p.Gln2054Pro) c.1160A>C (p.Gln387Pro) c.*1924A>C (n.*1924A>C) c.1468A>C n.281A>C | |
| 15 | g.48441723T= | CA2175508593 | FBN1 | c.6161A= (p.Gln2054=) c.1160A= (p.Gln387=) c.*1924A= (n.*1924A=) c.1468A= n.281A= | |
| 15 | g.48441724G>A | CA392337890 | FBN1 | c.6160C>T (p.Gln2054Ter) c.1159C>T (p.Gln387Ter) c.*1923C>T (n.*1923C>T) c.1467C>T n.280C>T | ClinVar dbSNP |
| 15 | g.48441724G>C | CA392337886 | FBN1 | c.6160C>G (p.Gln2054Glu) c.1159C>G (p.Gln387Glu) c.*1923C>G (n.*1923C>G) c.1467C>G n.280C>G | |
| 15 | g.48441724G= | CA2175508600 | FBN1 | c.6160C= (p.Gln2054=) c.1159C= (p.Gln387=) c.*1923C= (n.*1923C=) c.1467C= n.280C= | |
| 15 | g.48441724G>T | CA392337884 | FBN1 | c.6160C>A (p.Gln2054Lys) c.1159C>A (p.Gln387Lys) c.*1923C>A (n.*1923C>A) c.1467C>A n.280C>A | |
| 15 | g.48441725G>A | CA490021256 | FBN1 | c.6159C>T (p.Cys2053=) c.1158C>T (p.Cys386=) c.*1922C>T (n.*1922C>T) c.1466C>T n.279C>T |