Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
5 | g.177993032G>A | CA340722 | PROP1 | c.358C>T (p.Arg120Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
5 | g.177993032G>C | CA362378891 | PROP1 | c.358C>G (p.Arg120Gly) | |
5 | g.177993032G= | CA1603814092 | PROP1 | c.358C= (p.Arg120=) | |
5 | g.177993032G>T | CA362378890 | PROP1 | c.358C>A (p.Arg120Ser) | |
5 | g.177993033G>A | CA3587535 | PROP1 | c.357C>T (p.Asn119=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.177993033G>C | CA362378892 | PROP1 | c.357C>G (p.Asn119Lys) | |
5 | g.177993033G= | CA1603814093 | PROP1 | c.357C= (p.Asn119=) | |
5 | g.177993033G>T | CA362378893 | PROP1 | c.357C>A (p.Asn119Lys) | |
5 | g.177993034T>A | CA362378894 | PROP1 | c.356A>T (p.Asn119Ile) | |
5 | g.177993034T>C | CA362378895 | PROP1 | c.356A>G (p.Asn119Ser) | |
5 | g.177993034T>G | CA362378896 | PROP1 | c.356A>C (p.Asn119Thr) | |
5 | g.177993035T>A | CA362378897 | PROP1 | c.355A>T (p.Asn119Tyr) | |
5 | g.177993035T>C | CA362378898 | PROP1 | c.355A>G (p.Asn119Asp) | |
5 | g.177993035T>G | CA362378899 | PROP1 | c.355A>C (p.Asn119His) | |
5 | g.177993036C>A | CA362378900 | PROP1 | c.354G>T (p.Gln118His) | |
5 | g.177993036C>G | CA362378901 | PROP1 | c.354G>C (p.Gln118His) | |
5 | g.177993036C>T | CA448355538 | PROP1 | c.354G>A (p.Gln118=) | ClinVar |
5 | g.177993037T>A | CA362378904 | PROP1 | c.353A>T (p.Gln118Leu) | |
5 | g.177993037T>C | CA362378903 | PROP1 | c.353A>G (p.Gln118Arg) | |
5 | g.177993037T>G | CA362378902 | PROP1 | c.353A>C (p.Gln118Pro) | |
5 | g.177993038G>A | CA362378905 | PROP1 | c.352C>T (p.Gln118Ter) | ClinVar dbSNP |
5 | g.177993038G>C | CA362378906 | PROP1 | c.352C>G (p.Gln118Glu) | |
5 | g.177993038G>T | CA362378907 | PROP1 | c.352C>A (p.Gln118Lys) | |
5 | g.177993039G>A | CA448355549 | PROP1 | c.351C>T (p.Phe117=) | |
5 | g.177993039G>C | CA362378908 | PROP1 | c.351C>G (p.Phe117Leu) | |
5 | g.177993039G>T | CA362378909 | PROP1 | c.351C>A (p.Phe117Leu) | |
5 | g.177993040A>C | CA362378910 | PROP1 | c.350T>G (p.Phe117Cys) | |
5 | g.177993040A>G | CA362378911 | PROP1 | c.350T>C (p.Phe117Ser) | |
5 | g.177993040A>T | CA362378912 | PROP1 | c.350T>A (p.Phe117Tyr) | |
5 | g.177993041A= | CA1603814094 | PROP1 | c.349T= (p.Phe117=) | |
5 | g.177993041A>C | CA362378913 | PROP1 | c.349T>G (p.Phe117Val) | |
5 | g.177993041A>G | CA3587536 | PROP1 | c.349T>C (p.Phe117Leu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
5 | g.177993041A>T | CA340724 | PROP1 | c.349T>A (p.Phe117Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.177993042C>A | CA362378916 | PROP1 | c.348G>T (p.Trp116Cys) | |
5 | g.177993042C>G | CA362378915 | PROP1 | c.348G>C (p.Trp116Cys) | |
5 | g.177993042C>T | CA362378914 | PROP1 | c.348G>A (p.Trp116Ter) | |
5 | g.177993043C>A | CA362378917 | PROP1 | c.347G>T (p.Trp116Leu) | |
5 | g.177993043C>G | CA362378918 | PROP1 | c.347G>C (p.Trp116Ser) | |
5 | g.177993043C>T | CA362378919 | PROP1 | c.347G>A (p.Trp116Ter) | |
5 | g.177993044A>C | CA362378920 | PROP1 | c.346T>G (p.Trp116Gly) | |
5 | g.177993044A>G | CA362378921 | PROP1 | c.346T>C (p.Trp116Arg) | |
5 | g.177993044A>T | CA362378922 | PROP1 | c.346T>A (p.Trp116Arg) | |
5 | g.177993045G>A | CA448355573 | PROP1 | c.345C>T (p.Val115=) | |
5 | g.177993045G>C | CA448355575 | PROP1 | c.345C>G (p.Val115=) | |
5 | g.177993045G>T | CA448355576 | PROP1 | c.345C>A (p.Val115=) | gnomAD v4 COSMIC |
5 | g.177993046A>C | CA362378923 | PROP1 | c.344T>G (p.Val115Gly) | |
5 | g.177993046A>G | CA362378924 | PROP1 | c.344T>C (p.Val115Ala) | |
5 | g.177993046A>T | CA362378925 | PROP1 | c.344T>A (p.Val115Asp) | |
5 | g.177993047C>A | CA362378926 | PROP1 | c.343G>T (p.Val115Phe) | |
5 | g.177993047C>G | CA362378927 | PROP1 | c.343G>C (p.Val115Leu) |