Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.35284816C>A | CA405300640 | HAMP | c.118C>A (p.Gln40Lys) n.2300C>A | |
19 | g.35284816C>G | CA405300649 | HAMP | c.118C>G (p.Gln40Glu) n.2300C>G | |
19 | g.35284816C>T | CA405300655 | HAMP | c.118C>T (p.Gln40Ter) n.2300C>T | |
19 | g.35284817A= | CA2333586023 | HAMP | c.119A= (p.Gln40=) n.2301A= | |
19 | g.35284817A>C | CA405300658 | HAMP | c.119A>C (p.Gln40Pro) n.2301A>C | dbSNP |
19 | g.35284817A>G | CA405300659 | HAMP | c.119A>G (p.Gln40Arg) n.2301A>G | dbSNP gnomAD v4 |
19 | g.35284817A>T | CA405300660 | HAMP | c.119A>T (p.Gln40Leu) n.2301A>T | |
19 | g.35284818G>A | CA507041096 | HAMP | c.120G>A (p.Gln40=) n.2302G>A | |
19 | g.35284818G>C | CA405300662 | HAMP | c.120G>C (p.Gln40His) n.2302G>C | |
19 | g.35284818G>T | CA405300664 | HAMP | c.120G>T (p.Gln40His) n.2302G>T | |
19 | g.35284819G>A | CA405300667 | HAMP | c.121G>A (p.Asp41Asn) n.2303G>A | dbSNP gnomAD v4 |
19 | g.35284819G>C | CA405300677 | HAMP | c.121G>C (p.Asp41His) n.2303G>C | |
19 | g.35284819G= | CA2333586024 | HAMP | c.121G= (p.Asp41=) n.2303G= | |
19 | g.35284819G>T | CA405300690 | HAMP | c.121G>T (p.Asp41Tyr) n.2303G>T | |
19 | g.35284820A>C | CA405300696 | HAMP | c.122A>C (p.Asp41Ala) n.2304A>C | |
19 | g.35284820A>G | CA405300699 | HAMP | c.122A>G (p.Asp41Gly) n.2304A>G | |
19 | g.35284820A>T | CA405300694 | HAMP | c.122A>T (p.Asp41Val) n.2304A>T | |
19 | g.35284821C>A | CA405300702 | HAMP | c.123C>A (p.Asp41Glu) n.2305C>A | |
19 | g.35284821C>G | CA405300703 | HAMP | c.123C>G (p.Asp41Glu) n.2305C>G | |
19 | g.35284821C>T | CA507041122 | HAMP | c.123C>T (p.Asp41=) n.2305C>T | |
19 | g.35284821_35284823delinsCAG | CA2333586025 | HAMP | c.123_125delinsCAG (p.Asp41=) n.2305_2307delinsCAG | |
19 | g.35284822A>C | CA507041126 | HAMP | c.124A>C (p.Arg42=) n.2306A>C | |
19 | g.35284822A>G | CA405300708 | HAMP | c.124A>G (p.Arg42Gly) n.2306A>G | |
19 | g.35284822A>T | CA405300712 | HAMP | c.124A>T (p.Arg42Ter) n.2306A>T | |
19 | g.35284824_35284825del | CA881771442 | HAMP | c.126_127del (p.Arg42SerfsTer?) n.2308_2309del | dbSNP gnomAD v3 gnomAD v4 |
19 | g.35284823G>A | CA405300717 | HAMP | c.125G>A (p.Arg42Lys) n.2307G>A | |
19 | g.35284823G>C | CA405300725 | HAMP | c.125G>C (p.Arg42Thr) n.2307G>C | |
19 | g.35284823G>T | CA405300728 | HAMP | c.125G>T (p.Arg42Ile) n.2307G>T | |
19 | g.35284824A>C | CA405300731 | HAMP | c.126A>C (p.Arg42Ser) n.2308A>C | |
19 | g.35284824A>G | CA507041133 | HAMP | c.126A>G (p.Arg42=) n.2308A>G | |
19 | g.35284824A>T | CA405300734 | HAMP | c.126A>T (p.Arg42Ser) n.2308A>T | |
19 | g.35284825G>A | CA405300738 | HAMP | c.127G>A (p.Ala43Thr) n.2309G>A | dbSNP gnomAD v3 gnomAD v4 |
19 | g.35284825G>C | CA405300740 | HAMP | c.127G>C (p.Ala43Pro) n.2309G>C | |
19 | g.35284825G= | CA2333586026 | HAMP | c.127G= (p.Ala43=) n.2309G= | |
19 | g.35284825G>T | CA405300745 | HAMP | c.127G>T (p.Ala43Ser) n.2309G>T | |
19 | g.35284826C>A | CA405300748 | HAMP | c.128C>A (p.Ala43Asp) n.2310C>A | dbSNP |
19 | g.35284826C= | CA2333586027 | HAMP | c.128C= (p.Ala43=) n.2310C= | |
19 | g.35284826C>G | CA405300757 | HAMP | c.128C>G (p.Ala43Gly) n.2310C>G | gnomAD v4 |
19 | g.35284826C>T | CA9375795 | HAMP | c.128C>T (p.Ala43Val) n.2310C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.35284827T>A | CA507041146 | HAMP | c.129T>A (p.Ala43=) n.2311T>A | |
19 | g.35284827T>C | CA507041148 | HAMP | c.129T>C (p.Ala43=) n.2311T>C | dbSNP gnomAD v2 gnomAD v4 |
19 | g.35284827T>G | CA507041151 | HAMP | c.129T>G (p.Ala43=) n.2311T>G | |
19 | g.35284827T= | CA2333586028 | HAMP | c.129T= (p.Ala43=) n.2311T= | |
19 | g.35284828G>A | CA405300763 | HAMP | c.130G>A (p.Gly44Arg) n.2312G>A | gnomAD v4 |
19 | g.35284828G>C | CA405300765 | HAMP | c.130G>C (p.Gly44Arg) n.2312G>C | |
19 | g.35284828G>T | CA405300760 | HAMP | c.130G>T (p.Gly44Ter) n.2312G>T | |
19 | g.35284829G>A | CA405300771 | HAMP | c.131G>A (p.Gly44Glu) n.2313G>A | |
19 | g.35284829G>C | CA405300770 | HAMP | c.131G>C (p.Gly44Ala) n.2313G>C | |
19 | g.35284829G>T | CA405300773 | HAMP | c.131G>T (p.Gly44Val) n.2313G>T | |
19 | g.35284830A>C | CA507041155 | HAMP | c.132A>C (p.Gly44=) n.2314A>C |