Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.47576222C>A | CA412826536 | SYN1 | c.1067G>T (p.Trp356Leu) | gnomAD v4 |
X | g.47576222C= | CA2427971887 | SYN1 | c.1067G= (p.Trp356=) | |
X | g.47576222C>G | CA412826533 | SYN1 | c.1067G>C (p.Trp356Ser) | |
X | g.47576222C>T | CA120799 | SYN1 | c.1067G>A (p.Trp356Ter) | ClinVar dbSNP |
X | g.47576223A>C | CA412826537 | SYN1 | c.1066T>G (p.Trp356Gly) | |
X | g.47576223A>G | CA412826540 | SYN1 | c.1066T>C (p.Trp356Arg) | |
X | g.47576223A>T | CA412826542 | SYN1 | c.1066T>A (p.Trp356Arg) | |
X | g.47576224C>A | CA515992672 | SYN1 | c.1065G>T (p.Leu355=) | |
X | g.47576224C= | CA2427971888 | SYN1 | c.1065G= (p.Leu355=) | |
X | g.47576224C>G | CA515992674 | SYN1 | c.1065G>C (p.Leu355=) | |
X | g.47576224C>T | CA515992675 | SYN1 | c.1065G>A (p.Leu355=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.47576225A>C | CA412826543 | SYN1 | c.1064T>G (p.Leu355Arg) | |
X | g.47576225A>G | CA412826544 | SYN1 | c.1064T>C (p.Leu355Pro) | |
X | g.47576225A>T | CA412826546 | SYN1 | c.1064T>A (p.Leu355Gln) | |
X | g.47576226G>A | CA10398414 | SYN1 | c.1063C>T (p.Leu355=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.47576226G>C | CA412826547 | SYN1 | c.1063C>G (p.Leu355Val) | |
X | g.47576226G= | CA2427971889 | SYN1 | c.1063C= (p.Leu355=) | |
X | g.47576226G>T | CA412826549 | SYN1 | c.1063C>A (p.Leu355Met) | |
X | g.47576227C>A | CA412826552 | SYN1 | c.1062G>T (p.Lys354Asn) | gnomAD v4 |
X | g.47576227C>G | CA412826555 | SYN1 | c.1062G>C (p.Lys354Asn) | |
X | g.47576227C>T | CA515992698 | SYN1 | c.1062G>A (p.Lys354=) | gnomAD v4 |
X | g.47576228T>A | CA412826556 | SYN1 | c.1061A>T (p.Lys354Met) | |
X | g.47576228T>C | CA412826558 | SYN1 | c.1061A>G (p.Lys354Arg) | |
X | g.47576228T>G | CA412826559 | SYN1 | c.1061A>C (p.Lys354Thr) | |
X | g.47576229T>A | CA412826562 | SYN1 | c.1060A>T (p.Lys354Ter) | |
X | g.47576229T>C | CA412826565 | SYN1 | c.1060A>G (p.Lys354Glu) | |
X | g.47576229T>G | CA412826563 | SYN1 | c.1060A>C (p.Lys354Gln) | |
X | g.47576230G>A | CA515992706 | SYN1 | c.1059C>T (p.Tyr353=) | |
X | g.47576230G>C | CA412826566 | SYN1 | c.1059C>G (p.Tyr353Ter) | |
X | g.47576230G>T | CA412826568 | SYN1 | c.1059C>A (p.Tyr353Ter) | |
X | g.47576231T>A | CA412826569 | SYN1 | c.1058A>T (p.Tyr353Phe) | |
X | g.47576231T>C | CA412826571 | SYN1 | c.1058A>G (p.Tyr353Cys) | |
X | g.47576231T>G | CA412826573 | SYN1 | c.1058A>C (p.Tyr353Ser) | |
X | g.47576232A>C | CA412826574 | SYN1 | c.1057T>G (p.Tyr353Asp) | |
X | g.47576232A>G | CA412826576 | SYN1 | c.1057T>C (p.Tyr353His) | |
X | g.47576232A>T | CA412826577 | SYN1 | c.1057T>A (p.Tyr353Asn) | |
X | g.47576233T>A | CA412826579 | SYN1 | c.1056A>T (p.Arg352Ser) | gnomAD v4 |
X | g.47576233T>C | CA515992717 | SYN1 | c.1056A>G (p.Arg352=) | |
X | g.47576233T>G | CA412826581 | SYN1 | c.1056A>C (p.Arg352Ser) | |
X | g.47576234C>A | CA412826585 | SYN1 | c.1056-1G>T (n.1056-1G>T) | dbSNP gnomAD v4 |
X | g.47576234C>G | CA412826584 | SYN1 | c.1056-1G>C (n.1056-1G>C) | |
X | g.47576234C>T | CA412826583 | SYN1 | c.1056-1G>A (n.1056-1G>A) | |
X | g.47576235T>A | CA412826586 | SYN1 | c.1056-2A>T (n.1056-2A>T) | |
X | g.47576235T>C | CA412826590 | SYN1 | c.1056-2A>G (n.1056-2A>G) | |
X | g.47576235T>G | CA412826588 | SYN1 | c.1056-2A>C (n.1056-2A>C) | |
X | g.47576238C>A | CA641900925 | SYN1 | c.1056-5G>T (n.1056-5G>T) | dbSNP gnomAD v2 gnomAD v4 |
X | g.47576238C= | CA2427971890 | SYN1 | c.1056-5G= (n.1056-5G=) | |
X | g.47576239A>G | CA2693585703 | SYN1 | c.1056-6T>C (n.1056-6T>C) | gnomAD v4 |
X | g.47576240A= | CA2427971893 | SYN1 | c.1056-7T= (n.1056-7T=) | |
X | g.47576240A>C | CA875821536 | SYN1 | c.1056-7T>G (n.1056-7T>G) | ClinVar dbSNP gnomAD v3 gnomAD v4 |