Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
22 | g.50625138G>A | CA640358550 | ARSA | c.*7C>T (n.*7C>T) c.180+225C>T c.*270C>T (n.*270C>T) | dbSNP gnomAD v2 gnomAD v4 |
22 | g.50625138G= | CA2410958334 | ARSA | c.*7C= (n.*7C=) c.180+225C= c.*270C= (n.*270C=) | |
22 | g.50625138G>T | CA2657590623 | ARSA | c.*7C>A (n.*7C>A) c.180+225C>A c.*270C>A (n.*270C>A) | gnomAD v4 |
22 | g.50625139G>A | CA2657590625 | ARSA | c.*6C>T (n.*6C>T) c.180+224C>T c.*269C>T (n.*269C>T) | gnomAD v4 |
22 | g.50625139G>T | CA2657590624 | ARSA | c.*6C>A (n.*6C>A) c.180+224C>A c.*269C>A (n.*269C>A) | gnomAD v4 |
22 | g.50625140G>A | CA2657590626 | ARSA | c.*5C>T (n.*5C>T) c.180+223C>T c.*268C>T (n.*268C>T) | gnomAD v4 |
22 | g.50625140G>T | CA2657590627 | ARSA | c.*5C>A (n.*5C>A) c.180+223C>A c.*268C>A (n.*268C>A) | gnomAD v4 |
22 | g.50625141G>A | CA2657590628 | ARSA | c.*4C>T (n.*4C>T) c.180+222C>T c.*267C>T (n.*267C>T) | gnomAD v4 |
22 | g.50625141G>T | CA2657590629 | ARSA | c.*4C>A (n.*4C>A) c.180+222C>A c.*267C>A (n.*267C>A) | gnomAD v4 |
22 | g.50625142C>A | CA2657590631 | ARSA | c.*3G>T (n.*3G>T) c.180+221G>T c.*266G>T (n.*266G>T) | gnomAD v4 |
22 | g.50625142C= | CA2410958335 | ARSA | c.*3G= (n.*3G=) c.180+221G= c.*266G= (n.*266G=) | |
22 | g.50625142C>G | CA2657590632 | ARSA | c.*3G>C (n.*3G>C) c.180+221G>C c.*266G>C (n.*266G>C) | gnomAD v4 |
22 | g.50625142C>T | CA640358551 | ARSA | c.*3G>A (n.*3G>A) c.180+221G>A c.*266G>A (n.*266G>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
22 | g.50625144del | CA2657590630 | ARSA | c.*3del (n.*3del) c.180+221del c.*266del (n.*266del) | gnomAD v4 |
22 | g.50625143C= | CA2410958336 | ARSA | c.*2G= (n.*2G=) c.180+220G= c.*265G= (n.*265G=) | |
22 | g.50625143C>T | CA325531145 | ARSA | c.*2G>A (n.*2G>A) c.180+220G>A c.*265G>A (n.*265G>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
22 | g.50625144C>A | CA2657590633 | ARSA | c.*1G>T (n.*1G>T) c.180+219G>T c.*264G>T (n.*264G>T) | gnomAD v4 |
22 | g.50625144C>T | CA2657590634 | ARSA | c.*1G>A (n.*1G>A) c.180+219G>A c.*264G>A (n.*264G>A) | gnomAD v4 |
22 | g.50625145T>A | CA412166545 | ARSA | c.1530A>T (p.Ter510Cys) c.1272A>T (p.Ter424Cys) c.180+218A>T c.*263A>T (n.*263A>T) c.1644A>T (p.Ter548Cys) | gnomAD v4 |
22 | g.50625145T>C | CA412166546 | ARSA | c.1530A>G (p.Ter510Trp) c.1272A>G (p.Ter424Trp) c.180+218A>G c.*263A>G (n.*263A>G) c.1644A>G (p.Ter548Trp) | gnomAD v4 |
22 | g.50625145T>G | CA412166547 | ARSA | c.1530A>C (p.Ter510Cys) c.1272A>C (p.Ter424Cys) c.180+218A>C c.*263A>C (n.*263A>C) c.1644A>C (p.Ter548Cys) | |
22 | g.50625146C>A | CA412166551 | ARSA | c.1529G>T (p.Ter510Leu) c.1271G>T (p.Ter424Leu) c.180+217G>T c.*262G>T (n.*262G>T) c.1643G>T (p.Ter548Leu) | gnomAD v4 |
22 | g.50625146C>G | CA412166549 | ARSA | c.1529G>C (p.Ter510Ser) c.1271G>C (p.Ter424Ser) c.180+217G>C c.*262G>C (n.*262G>C) c.1643G>C (p.Ter548Ser) | |
22 | g.50625146C>T | CA515390741 | ARSA | c.1529G>A (p.Ter510=) c.1271G>A (p.Ter424=) c.180+217G>A c.*262G>A (n.*262G>A) c.1643G>A (p.Ter548=) | gnomAD v4 |
22 | g.50625147A>C | CA412166558 | ARSA | c.1528T>G (p.Ter510Gly) c.1270T>G (p.Ter424Gly) c.180+216T>G c.*261T>G (n.*261T>G) c.1642T>G (p.Ter548Gly) | |
22 | g.50625147A>G | CA412166561 | ARSA | c.1528T>C (p.Ter510Arg) c.1270T>C (p.Ter424Arg) c.180+216T>C c.*261T>C (n.*261T>C) c.1642T>C (p.Ter548Arg) | ClinVar gnomAD v4 |
22 | g.50625147A>T | CA412166563 | ARSA | c.1528T>A (p.Ter510Arg) c.1270T>A (p.Ter424Arg) c.180+216T>A c.*261T>A (n.*261T>A) c.1642T>A (p.Ter548Arg) | |
22 | g.50625148G>A | CA515390746 | ARSA | c.1527C>T (p.Ala509=) c.1269C>T (p.Ala423=) c.180+215C>T c.*260C>T (n.*260C>T) c.1641C>T (p.Ala547=) | gnomAD v4 |
22 | g.50625148G>C | CA515390743 | ARSA | c.1527C>G (p.Ala509=) c.1269C>G (p.Ala423=) c.180+215C>G c.*260C>G (n.*260C>G) c.1641C>G (p.Ala547=) | gnomAD v4 |
22 | g.50625148G= | CA2410958337 | ARSA | c.1527C= (p.Ala509=) c.1269C= (p.Ala423=) c.180+215C= c.*260C= (n.*260C=) c.1641C= (p.Ala547=) | |
22 | g.50625148G>T | CA515390745 | ARSA | c.1527C>A (p.Ala509=) c.1269C>A (p.Ala423=) c.180+215C>A c.*260C>A (n.*260C>A) c.1641C>A (p.Ala547=) | ClinVar dbSNP gnomAD v4 |
22 | g.50625149G>A | CA412166564 | ARSA | c.1526C>T (p.Ala509Val) c.1268C>T (p.Ala423Val) c.180+214C>T c.*259C>T (n.*259C>T) c.1640C>T (p.Ala547Val) | gnomAD v4 |
22 | g.50625149G>C | CA412166566 | ARSA | c.1526C>G (p.Ala509Gly) c.1268C>G (p.Ala423Gly) c.180+214C>G c.*259C>G (n.*259C>G) c.1640C>G (p.Ala547Gly) | gnomAD v4 |
22 | g.50625149G>T | CA412166568 | ARSA | c.1526C>A (p.Ala509Asp) c.1268C>A (p.Ala423Asp) c.180+214C>A c.*259C>A (n.*259C>A) c.1640C>A (p.Ala547Asp) | gnomAD v4 |
22 | g.50625150C>A | CA412166573 | ARSA | c.1525G>T (p.Ala509Ser) c.1267G>T (p.Ala423Ser) c.180+213G>T c.*258G>T (n.*258G>T) c.1639G>T (p.Ala547Ser) | gnomAD v4 |
22 | g.50625150C>G | CA412166570 | ARSA | c.1525G>C (p.Ala509Pro) c.1267G>C (p.Ala423Pro) c.180+213G>C c.*258G>C (n.*258G>C) c.1639G>C (p.Ala547Pro) | gnomAD v4 |
22 | g.50625150C>T | CA412166571 | ARSA | c.1525G>A (p.Ala509Thr) c.1267G>A (p.Ala423Thr) c.180+213G>A c.*258G>A (n.*258G>A) c.1639G>A (p.Ala547Thr) | gnomAD v4 |
22 | g.50625151A= | CA2410958338 | ARSA | c.1524T= (p.His508=) c.1266T= (p.His422=) c.180+212T= c.*257T= (n.*257T=) c.1638T= (p.His546=) | |
22 | g.50625151A>C | CA10324714 | ARSA | c.1524T>G (p.His508Gln) c.1266T>G (p.His422Gln) c.180+212T>G c.*257T>G (n.*257T>G) c.1638T>G (p.His546Gln) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
22 | g.50625151A>G | CA515390754 | ARSA | c.1524T>C (p.His508=) c.1266T>C (p.His422=) c.180+212T>C c.*257T>C (n.*257T>C) c.1638T>C (p.His546=) | |
22 | g.50625151A>T | CA412166580 | ARSA | c.1524T>A (p.His508Gln) c.1266T>A (p.His422Gln) c.180+212T>A c.*257T>A (n.*257T>A) c.1638T>A (p.His546Gln) | |
22 | g.50625152T>A | CA412166584 | ARSA | c.1523A>T (p.His508Leu) c.1265A>T (p.His422Leu) c.180+211A>T c.*256A>T (n.*256A>T) c.1637A>T (p.His546Leu) | |
22 | g.50625152T>C | CA412166587 | ARSA | c.1523A>G (p.His508Arg) c.1265A>G (p.His422Arg) c.180+211A>G c.*256A>G (n.*256A>G) c.1637A>G (p.His546Arg) | ClinVar dbSNP gnomAD v4 |
22 | g.50625152T>G | CA412166591 | ARSA | c.1523A>C (p.His508Pro) c.1265A>C (p.His422Pro) c.180+211A>C c.*256A>C (n.*256A>C) c.1637A>C (p.His546Pro) | |
22 | g.50625152T= | CA2410958339 | ARSA | c.1523A= (p.His508=) c.1265A= (p.His422=) c.180+211A= c.*256A= (n.*256A=) c.1637A= (p.His546=) | |
22 | g.50625153G>A | CA412166594 | ARSA | c.1522C>T (p.His508Tyr) c.1264C>T (p.His422Tyr) c.180+210C>T c.*255C>T (n.*255C>T) c.1636C>T (p.His546Tyr) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
22 | g.50625153G>C | CA412166599 | ARSA | c.1522C>G (p.His508Asp) c.1264C>G (p.His422Asp) c.180+210C>G c.*255C>G (n.*255C>G) c.1636C>G (p.His546Asp) | |
22 | g.50625153G= | CA2410958340 | ARSA | c.1522C= (p.His508=) c.1264C= (p.His422=) c.180+210C= c.*255C= (n.*255C=) c.1636C= (p.His546=) | |
22 | g.50625153G>T | CA412166596 | ARSA | c.1522C>A (p.His508Asn) c.1264C>A (p.His422Asn) c.180+210C>A c.*255C>A (n.*255C>A) c.1636C>A (p.His546Asn) | gnomAD v4 |
22 | g.50625156del | CA2657590635 | ARSA | c.1522del (p.His508MetfsTer12) c.1264del (p.His422MetfsTer12) c.180+210del c.*255del (n.*255del) c.1636del (p.His546MetfsTer12) | gnomAD v4 |