Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.35284936A= | CA2333586096 | HAMP | c.151-2A= (n.151-2A=) n.2420A= | |
19 | g.35284936A>C | CA405301053 | HAMP | c.151-2A>C (n.151-2A>C) n.2420A>C | |
19 | g.35284936A>G | CA405301057 | HAMP | c.151-2A>G (n.151-2A>G) n.2420A>G | |
19 | g.35284936A>T | CA307740334 | HAMP | c.151-2A>T (n.151-2A>T) n.2420A>T | dbSNP |
19 | g.35284937G>A | CA9375820 | HAMP | c.151-1G>A (n.151-1G>A) n.2421G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.35284937G>C | CA405301068 | HAMP | c.151-1G>C (n.151-1G>C) n.2421G>C | dbSNP gnomAD v4 |
19 | g.35284937G= | CA2333586097 | HAMP | c.151-1G= (n.151-1G=) n.2421G= | |
19 | g.35284937G>T | CA405301070 | HAMP | c.151-1G>T (n.151-1G>T) n.2421G>T | COSMIC |
19 | g.35284938C>A | CA405301074 | HAMP | c.151C>A (p.Pro51Thr) n.2422C>A | |
19 | g.35284938C= | CA2333586098 | HAMP | c.151C= (p.Pro51=) n.2422C= | |
19 | g.35284938C>G | CA405301075 | HAMP | c.151C>G (p.Pro51Ala) n.2422C>G | dbSNP |
19 | g.35284938C>T | CA405301076 | HAMP | c.151C>T (p.Pro51Ser) n.2422C>T | dbSNP gnomAD v2 gnomAD v4 |
19 | g.35284939C>A | CA405301079 | HAMP | c.152C>A (p.Pro51His) n.2423C>A | |
19 | g.35284939C>G | CA405301081 | HAMP | c.152C>G (p.Pro51Arg) n.2423C>G | |
19 | g.35284939C>T | CA405301087 | HAMP | c.152C>T (p.Pro51Leu) n.2423C>T | gnomAD v4 |
19 | g.35284940C>A | CA507041329 | HAMP | c.153C>A (p.Pro51=) n.2424C>A | |
19 | g.35284940C>G | CA507041331 | HAMP | c.153C>G (p.Pro51=) n.2424C>G | |
19 | g.35284940C>T | CA507041332 | HAMP | c.153C>T (p.Pro51=) n.2424C>T | |
19 | g.35284941A= | CA2333586099 | HAMP | c.154A= (p.Met52=) n.2425A= | |
19 | g.35284941A>C | CA405301097 | HAMP | c.154A>C (p.Met52Leu) n.2425A>C | |
19 | g.35284941A>G | CA9375821 | HAMP | c.154A>G (p.Met52Val) n.2425A>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.35284941A>T | CA405301091 | HAMP | c.154A>T (p.Met52Leu) n.2425A>T | |
19 | g.35284942del | CA2584453480 | HAMP | c.155del (p.Met52SerfsTer?) n.2426del | gnomAD v4 |
19 | g.35284942T>A | CA405301100 | HAMP | c.155T>A (p.Met52Lys) n.2426T>A | |
19 | g.35284942T>C | CA9375822 | HAMP | c.155T>C (p.Met52Thr) n.2426T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.35284942T>G | CA405301104 | HAMP | c.155T>G (p.Met52Arg) n.2426T>G | |
19 | g.35284942T= | CA2333586100 | HAMP | c.155T= (p.Met52=) n.2426T= | |
19 | g.35284943G>A | CA307740366 | HAMP | c.156G>A (p.Met52Ile) n.2427G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.35284943G>C | CA405301112 | HAMP | c.156G>C (p.Met52Ile) n.2427G>C | |
19 | g.35284943G= | CA2333586101 | HAMP | c.156G= (p.Met52=) n.2427G= | |
19 | g.35284943G>T | CA405301115 | HAMP | c.156G>T (p.Met52Ile) n.2427G>T | gnomAD v4 |
19 | g.35284944T>A | CA405301119 | HAMP | c.157T>A (p.Phe53Ile) n.2428T>A | |
19 | g.35284944T>C | CA405301123 | HAMP | c.157T>C (p.Phe53Leu) n.2428T>C | dbSNP gnomAD v4 |
19 | g.35284944T>G | CA405301126 | HAMP | c.157T>G (p.Phe53Val) n.2428T>G | |
19 | g.35284945T>A | CA405301127 | HAMP | c.158T>A (p.Phe53Tyr) n.2429T>A | |
19 | g.35284945T>C | CA405301128 | HAMP | c.158T>C (p.Phe53Ser) n.2429T>C | |
19 | g.35284945T>G | CA405301129 | HAMP | c.158T>G (p.Phe53Cys) n.2429T>G | |
19 | g.35284946C>A | CA405301131 | HAMP | c.159C>A (p.Phe53Leu) n.2430C>A | |
19 | g.35284946C= | CA2333586102 | HAMP | c.159C= (p.Phe53=) n.2430C= | |
19 | g.35284946C>G | CA405301132 | HAMP | c.159C>G (p.Phe53Leu) n.2430C>G | |
19 | g.35284946C>T | CA307740386 | HAMP | c.159C>T (p.Phe53=) n.2430C>T | dbSNP gnomAD v4 |
19 | g.35284947C>A | CA307740388 | HAMP | c.160C>A (p.Gln54Lys) n.2431C>A | dbSNP gnomAD v4 |
19 | g.35284947C= | CA2333586103 | HAMP | c.160C= (p.Gln54=) n.2431C= | |
19 | g.35284947C>G | CA405301135 | HAMP | c.160C>G (p.Gln54Glu) n.2431C>G | |
19 | g.35284947C>T | CA405301138 | HAMP | c.160C>T (p.Gln54Ter) n.2431C>T | |
19 | g.35284948A= | CA2333586104 | HAMP | c.161A= (p.Gln54=) n.2432A= | |
19 | g.35284948A>C | CA307740389 | HAMP | c.161A>C (p.Gln54Pro) n.2432A>C | dbSNP |
19 | g.35284948A>G | CA405301146 | HAMP | c.161A>G (p.Gln54Arg) n.2432A>G | |
19 | g.35284948A>T | CA405301150 | HAMP | c.161A>T (p.Gln54Leu) n.2432A>T | |
19 | g.35284949G>A | CA507041350 | HAMP | c.162G>A (p.Gln54=) n.2433G>A | gnomAD v4 |
19 | g.35284949G>C | CA405301159 | HAMP | c.162G>C (p.Gln54His) n.2433G>C | COSMIC |
19 | g.35284949G>T | CA405301156 | HAMP | c.162G>T (p.Gln54His) n.2433G>T | |
19 | g.35284950A= | CA2333586105 | HAMP | c.163A= (p.Arg55=) n.2434A= | |
19 | g.35284950A>C | CA507041354 | HAMP | c.163A>C (p.Arg55=) n.2434A>C | |
19 | g.35284950A>G | CA307740390 | HAMP | c.163A>G (p.Arg55Gly) n.2434A>G | ClinVar dbSNP |
19 | g.35284950A>T | CA405301164 | HAMP | c.163A>T (p.Arg55Trp) n.2434A>T | |
19 | g.35284951G>A | CA405301165 | HAMP | c.164G>A (p.Arg55Lys) n.2435G>A | dbSNP gnomAD v3 gnomAD v4 |
19 | g.35284951G>C | CA405301166 | HAMP | c.164G>C (p.Arg55Thr) n.2435G>C | |
19 | g.35284951G= | CA2333586106 | HAMP | c.164G= (p.Arg55=) n.2435G= | |
19 | g.35284951G>T | CA405301167 | HAMP | c.164G>T (p.Arg55Met) n.2435G>T | COSMIC |
19 | g.35284952G>A | CA507041361 | HAMP | c.165G>A (p.Arg55=) n.2436G>A | gnomAD v4 |
19 | g.35284952G>C | CA405301168 | HAMP | c.165G>C (p.Arg55Ser) n.2436G>C | |
19 | g.35284952G>T | CA405301170 | HAMP | c.165G>T (p.Arg55Ser) n.2436G>T | gnomAD v4 |
19 | g.35284953C>A | CA507041374 | HAMP | c.166C>A (p.Arg56=) n.2437C>A | |
19 | g.35284953C= | CA2333586107 | HAMP | c.166C= (p.Arg56=) n.2437C= | |
19 | g.35284953C>G | CA405301171 | HAMP | c.166C>G (p.Arg56Gly) n.2437C>G | dbSNP |
19 | g.35284953C>T | CA253053 | HAMP | c.166C>T (p.Arg56Ter) n.2437C>T | ClinVar dbSNP gnomAD v4 COSMIC |
19 | g.35284954G>A | CA9375823 | HAMP | c.167G>A (p.Arg56Gln) n.2438G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
19 | g.35284954G>C | CA405301177 | HAMP | c.167G>C (p.Arg56Pro) n.2438G>C | |
19 | g.35284954G= | CA2333586108 | HAMP | c.167G= (p.Arg56=) n.2438G= | |
19 | g.35284954G>T | CA405301175 | HAMP | c.167G>T (p.Arg56Leu) n.2438G>T | dbSNP gnomAD v3 gnomAD v4 |
19 | g.35284955A>C | CA507041378 | HAMP | c.168A>C (p.Arg56=) n.2439A>C | |
19 | g.35284955A>G | CA507041379 | HAMP | c.168A>G (p.Arg56=) n.2439A>G | |
19 | g.35284955A>T | CA507041384 | HAMP | c.168A>T (p.Arg56=) n.2439A>T | |
19 | g.35284956A>C | CA507041388 | HAMP | c.169A>C (p.Arg57=) n.2440A>C | |
19 | g.35284956A>G | CA405301180 | HAMP | c.169A>G (p.Arg57Gly) n.2440A>G | |
19 | g.35284956A>T | CA405301184 | HAMP | c.169A>T (p.Arg57Trp) n.2440A>T | |
19 | g.35284957G>A | CA405301188 | HAMP | c.170G>A (p.Arg57Lys) n.2441G>A | dbSNP gnomAD v2 gnomAD v4 |
19 | g.35284957G>C | CA405301192 | HAMP | c.170G>C (p.Arg57Thr) n.2441G>C | |
19 | g.35284957G= | CA2333586109 | HAMP | c.170G= (p.Arg57=) n.2441G= | |
19 | g.35284957G>T | CA405301190 | HAMP | c.170G>T (p.Arg57Met) n.2441G>T | |
19 | g.35284958G>A | CA507041400 | HAMP | c.171G>A (p.Arg57=) n.2442G>A | gnomAD v4 |
19 | g.35284958G>C | CA405301193 | HAMP | c.171G>C (p.Arg57Ser) n.2442G>C | |
19 | g.35284958G>T | CA405301194 | HAMP | c.171G>T (p.Arg57Ser) n.2442G>T | |
19 | g.35284959A>C | CA507041412 | HAMP | c.172A>C (p.Arg58=) n.2443A>C | |
19 | g.35284959A>G | CA405301197 | HAMP | c.172A>G (p.Arg58Gly) n.2443A>G | |
19 | g.35284959A>T | CA405301203 | HAMP | c.172A>T (p.Arg58Trp) n.2443A>T | gnomAD v4 |
19 | g.35284960G>A | CA307740400 | HAMP | c.173G>A (p.Arg58Lys) n.2444G>A | dbSNP gnomAD v2 gnomAD v4 |
19 | g.35284960G>C | CA405301207 | HAMP | c.173G>C (p.Arg58Thr) n.2444G>C | |
19 | g.35284960G= | CA2333586110 | HAMP | c.173G= (p.Arg58=) n.2444G= | |
19 | g.35284960G>T | CA405301210 | HAMP | c.173G>T (p.Arg58Met) n.2444G>T | gnomAD v4 |
19 | g.35284961G>A | CA507041442 | HAMP | c.174G>A (p.Arg58=) n.2445G>A | |
19 | g.35284961G>C | CA405301217 | HAMP | c.174G>C (p.Arg58Ser) n.2445G>C | |
19 | g.35284961G>T | CA405301220 | HAMP | c.174G>T (p.Arg58Ser) n.2445G>T | |
19 | g.35284962C>A | CA507041457 | HAMP | c.175C>A (p.Arg59=) n.2446C>A | |
19 | g.35284962C= | CA2333586111 | HAMP | c.175C= (p.Arg59=) n.2446C= | |
19 | g.35284962C>G | CA9375824 | HAMP | c.175C>G (p.Arg59Gly) n.2446C>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.35284962C>T | CA405301225 | HAMP | c.175C>T (p.Arg59Ter) n.2446C>T | ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC |
19 | g.35284963G>A | CA405301227 | HAMP | c.176G>A (p.Arg59Gln) n.2447G>A | dbSNP gnomAD v3 gnomAD v4 |
19 | g.35284963G>C | CA405301228 | HAMP | c.176G>C (p.Arg59Pro) n.2447G>C | ClinVar dbSNP |
19 | g.35284963G= | CA2333586112 | HAMP | c.176G= (p.Arg59=) n.2447G= | |
19 | g.35284963G>T | CA405301229 | HAMP | c.176G>T (p.Arg59Leu) n.2447G>T | |
19 | g.35284964A>C | CA507041470 | HAMP | c.177A>C (p.Arg59=) n.2448A>C | |
19 | g.35284964A>G | CA507041471 | HAMP | c.177A>G (p.Arg59=) n.2448A>G | |
19 | g.35284964A>T | CA507041475 | HAMP | c.177A>T (p.Arg59=) n.2448A>T | |
19 | g.35284965G>A | CA405301235 | HAMP | c.178G>A (p.Asp60Asn) n.2449G>A | dbSNP gnomAD v3 gnomAD v4 |
19 | g.35284965G>C | CA405301233 | HAMP | c.178G>C (p.Asp60His) n.2449G>C | |
19 | g.35284965G= | CA2333586113 | HAMP | c.178G= (p.Asp60=) n.2449G= | |
19 | g.35284965G>T | CA405301230 | HAMP | c.178G>T (p.Asp60Tyr) n.2449G>T | |
19 | g.35284966A= | CA2333586114 | HAMP | c.179A= (p.Asp60=) n.2450A= | |
19 | g.35284966A>C | CA405301244 | HAMP | c.179A>C (p.Asp60Ala) n.2450A>C | |
19 | g.35284966A>G | CA405301246 | HAMP | c.179A>G (p.Asp60Gly) n.2450A>G | dbSNP gnomAD v3 gnomAD v4 |
19 | g.35284966A>T | CA405301251 | HAMP | c.179A>T (p.Asp60Val) n.2450A>T | dbSNP |
19 | g.35284967C>A | CA405301255 | HAMP | c.180C>A (p.Asp60Glu) n.2451C>A | |
19 | g.35284967C= | CA2333586115 | HAMP | c.180C= (p.Asp60=) n.2451C= | |
19 | g.35284967C>G | CA405301259 | HAMP | c.180C>G (p.Asp60Glu) n.2451C>G | |
19 | g.35284967C>T | CA307740407 | HAMP | c.180C>T (p.Asp60=) n.2451C>T | dbSNP gnomAD v2 gnomAD v4 |
19 | g.35284968A= | CA2333586116 | HAMP | c.181A= (p.Thr61=) n.2452A= | |
19 | g.35284968A>C | CA405301262 | HAMP | c.181A>C (p.Thr61Pro) n.2452A>C | |
19 | g.35284968A>G | CA405301277 | HAMP | c.181A>G (p.Thr61Ala) n.2452A>G | |
19 | g.35284968A>T | CA9375825 | HAMP | c.181A>T (p.Thr61Ser) n.2452A>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.35284969C>A | CA405301280 | HAMP | c.182C>A (p.Thr61Asn) n.2453C>A | COSMIC |
19 | g.35284969C>G | CA405301282 | HAMP | c.182C>G (p.Thr61Ser) n.2453C>G | |
19 | g.35284969C>T | CA405301285 | HAMP | c.182C>T (p.Thr61Ile) n.2453C>T | gnomAD v4 |
19 | g.35284970C>A | CA507041504 | HAMP | c.183C>A (p.Thr61=) n.2454C>A | gnomAD v4 |
19 | g.35284970C= | CA2333586117 | HAMP | c.183C= (p.Thr61=) n.2454C= | |
19 | g.35284970C>G | CA507041502 | HAMP | c.183C>G (p.Thr61=) n.2454C>G | dbSNP gnomAD v2 |
19 | g.35284970C>T | CA507041500 | HAMP | c.183C>T (p.Thr61=) n.2454C>T | dbSNP gnomAD v2 gnomAD v4 |
19 | g.35284971C>A | CA405301306 | HAMP | c.184C>A (p.His62Asn) n.2455C>A | |
19 | g.35284971C>G | CA405301310 | HAMP | c.184C>G (p.His62Asp) n.2455C>G | |
19 | g.35284971C>T | CA405301302 | HAMP | c.184C>T (p.His62Tyr) n.2455C>T | gnomAD v4 |
19 | g.35284972A>C | CA405301315 | HAMP | c.185A>C (p.His62Pro) n.2456A>C | |
19 | g.35284972A>G | CA405301316 | HAMP | c.185A>G (p.His62Arg) n.2456A>G | |
19 | g.35284972A>T | CA405301320 | HAMP | c.185A>T (p.His62Leu) n.2456A>T | |
19 | g.35284973C>A | CA405301331 | HAMP | c.186C>A (p.His62Gln) n.2457C>A | |
19 | g.35284973C>G | CA405301335 | HAMP | c.186C>G (p.His62Gln) n.2457C>G | |
19 | g.35284973C>T | CA507041532 | HAMP | c.186C>T (p.His62=) n.2457C>T | gnomAD v4 |
19 | g.35284974T>A | CA405301339 | HAMP | c.187T>A (p.Phe63Ile) n.2458T>A | |
19 | g.35284974T>C | CA405301344 | HAMP | c.187T>C (p.Phe63Leu) n.2458T>C | |
19 | g.35284974T>G | CA405301349 | HAMP | c.187T>G (p.Phe63Val) n.2458T>G | |
19 | g.35284975T>A | CA405301352 | HAMP | c.188T>A (p.Phe63Tyr) n.2459T>A | |
19 | g.35284975T>C | CA405301368 | HAMP | c.188T>C (p.Phe63Ser) n.2459T>C | |
19 | g.35284975T>G | CA405301371 | HAMP | c.188T>G (p.Phe63Cys) n.2459T>G | |
19 | g.35284976C>A | CA405301375 | HAMP | c.189C>A (p.Phe63Leu) n.2460C>A | |
19 | g.35284976C= | CA2333586118 | HAMP | c.189C= (p.Phe63=) n.2460C= | |
19 | g.35284976C>G | CA405301378 | HAMP | c.189C>G (p.Phe63Leu) n.2460C>G | |
19 | g.35284976C>T | CA307740438 | HAMP | c.189C>T (p.Phe63=) n.2460C>T | ClinVar dbSNP gnomAD v3 gnomAD v4 |
19 | g.35284977C>A | CA405301383 | HAMP | c.190C>A (p.Pro64Thr) n.2461C>A | |
19 | g.35284977C= | CA2333586119 | HAMP | c.190C= (p.Pro64=) n.2461C= | |
19 | g.35284977C>G | CA405301385 | HAMP | c.190C>G (p.Pro64Ala) n.2461C>G | dbSNP gnomAD v4 |
19 | g.35284977C>T | CA405301387 | HAMP | c.190C>T (p.Pro64Ser) n.2461C>T | gnomAD v4 COSMIC |
19 | g.35284978C>A | CA405301388 | HAMP | c.191C>A (p.Pro64His) n.2462C>A | |
19 | g.35284978C>G | CA405301389 | HAMP | c.191C>G (p.Pro64Arg) n.2462C>G | |
19 | g.35284978C>T | CA405301390 | HAMP | c.191C>T (p.Pro64Leu) n.2462C>T | |
19 | g.35284979C>A | CA507041568 | HAMP | c.192C>A (p.Pro64=) n.2463C>A | |
19 | g.35284979C>G | CA507041570 | HAMP | c.192C>G (p.Pro64=) n.2463C>G | |
19 | g.35284979C>T | CA507041572 | HAMP | c.192C>T (p.Pro64=) n.2463C>T | ClinVar |
19 | g.35284979_35284980insCAAACACACCCAACAC | CA2814241050 | HAMP | c.192_193insCAAACACACCCAACAC (p.Ile65GlnfsTer?) n.2463_2464insCAAACACACCCAACAC | |
19 | g.35284980A>C | CA405301391 | HAMP | c.193A>C (p.Ile65Leu) n.2464A>C | |
19 | g.35284980A>G | CA405301395 | HAMP | c.193A>G (p.Ile65Val) n.2464A>G | |
19 | g.35284980A>T | CA405301393 | HAMP | c.193A>T (p.Ile65Phe) n.2464A>T | |
19 | g.35284981T>A | CA405301398 | HAMP | c.194T>A (p.Ile65Asn) n.2465T>A | |
19 | g.35284981T>C | CA405301399 | HAMP | c.194T>C (p.Ile65Thr) n.2465T>C | dbSNP gnomAD v3 gnomAD v4 |
19 | g.35284981T>G | CA405301400 | HAMP | c.194T>G (p.Ile65Ser) n.2465T>G | |
19 | g.35284981T= | CA2333586120 | HAMP | c.194T= (p.Ile65=) n.2465T= | |
19 | g.35284982C>A | CA507041585 | HAMP | c.195C>A (p.Ile65=) n.2466C>A | |
19 | g.35284982C= | CA2333586121 | HAMP | c.195C= (p.Ile65=) n.2466C= | |
19 | g.35284982C>G | CA405301402 | HAMP | c.195C>G (p.Ile65Met) n.2466C>G | |
19 | g.35284982C>T | CA9375826 | HAMP | c.195C>T (p.Ile65=) n.2466C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.35284983T>A | CA405301409 | HAMP | c.196T>A (p.Cys66Ser) n.2467T>A | |
19 | g.35284983T>C | CA405301412 | HAMP | c.196T>C (p.Cys66Arg) n.2467T>C | dbSNP gnomAD v3 gnomAD v4 |
19 | g.35284983T>G | CA405301407 | HAMP | c.196T>G (p.Cys66Gly) n.2467T>G | |
19 | g.35284983T= | CA2333586122 | HAMP | c.196T= (p.Cys66=) n.2467T= | |
19 | g.35284984G>A | CA405301422 | HAMP | c.197G>A (p.Cys66Tyr) n.2468G>A | gnomAD v4 |
19 | g.35284984G>C | CA405301417 | HAMP | c.197G>C (p.Cys66Ser) n.2468G>C | |
19 | g.35284984G>T | CA405301420 | HAMP | c.197G>T (p.Cys66Phe) n.2468G>T | gnomAD v4 |
19 | g.35284985C>A | CA405301427 | HAMP | c.198C>A (p.Cys66Ter) n.2469C>A | |
19 | g.35284985C= | CA2333586123 | HAMP | c.198C= (p.Cys66=) n.2469C= | |
19 | g.35284985C>G | CA405301429 | HAMP | c.198C>G (p.Cys66Trp) n.2469C>G | |
19 | g.35284985C>T | CA507041596 | HAMP | c.198C>T (p.Cys66=) n.2469C>T | dbSNP |
19 | g.35284986A>C | CA405301431 | HAMP | c.199A>C (p.Ile67Leu) n.2470A>C | |
19 | g.35284986A>G | CA405301434 | HAMP | c.199A>G (p.Ile67Val) n.2470A>G | |
19 | g.35284986A>T | CA405301436 | HAMP | c.199A>T (p.Ile67Phe) n.2470A>T | |
19 | g.35284987T>A | CA405301439 | HAMP | c.200T>A (p.Ile67Asn) n.2471T>A | |
19 | g.35284987T>C | CA405301443 | HAMP | c.200T>C (p.Ile67Thr) n.2471T>C | |
19 | g.35284987T>G | CA9375827 | HAMP | c.200T>G (p.Ile67Ser) n.2471T>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.35284987T= | CA2333586124 | HAMP | c.200T= (p.Ile67=) n.2471T= | |
19 | g.35284988T>A | CA507041605 | HAMP | c.201T>A (p.Ile67=) n.2472T>A | |
19 | g.35284988T>C | CA507041607 | HAMP | c.201T>C (p.Ile67=) n.2472T>C | |
19 | g.35284988T>G | CA405301450 | HAMP | c.201T>G (p.Ile67Met) n.2472T>G | |
19 | g.35284989T>A | CA405301452 | HAMP | c.202T>A (p.Phe68Ile) n.2473T>A | |
19 | g.35284989T>C | CA405301455 | HAMP | c.202T>C (p.Phe68Leu) n.2473T>C | |
19 | g.35284989T>G | CA405301457 | HAMP | c.202T>G (p.Phe68Val) n.2473T>G | |
19 | g.35284990T>A | CA405301458 | HAMP | c.203T>A (p.Phe68Tyr) n.2474T>A | |
19 | g.35284990T>C | CA405301460 | HAMP | c.203T>C (p.Phe68Ser) n.2474T>C | |
19 | g.35284990T>G | CA405301459 | HAMP | c.203T>G (p.Phe68Cys) n.2474T>G | |
19 | g.35284991C>A | CA405301461 | HAMP | c.204C>A (p.Phe68Leu) n.2475C>A | |
19 | g.35284991C>G | CA405301462 | HAMP | c.204C>G (p.Phe68Leu) n.2475C>G | |
19 | g.35284991C>T | CA507041618 | HAMP | c.204C>T (p.Phe68=) n.2475C>T | |
19 | g.35284992T>A | CA405301465 | HAMP | c.205T>A (p.Cys69Ser) n.2476T>A | |
19 | g.35284992T>C | CA405301475 | HAMP | c.205T>C (p.Cys69Arg) n.2476T>C | |
19 | g.35284992T>G | CA405301480 | HAMP | c.205T>G (p.Cys69Gly) n.2476T>G | |
19 | g.35284993G>A | CA405301483 | HAMP | c.206G>A (p.Cys69Tyr) n.2477G>A | |
19 | g.35284993G>C | CA405301488 | HAMP | c.206G>C (p.Cys69Ser) n.2477G>C | |
19 | g.35284993G>T | CA405301490 | HAMP | c.206G>T (p.Cys69Phe) n.2477G>T | gnomAD v4 COSMIC |
19 | g.35284994C>A | CA405301492 | HAMP | c.207C>A (p.Cys69Ter) n.2478C>A | |
19 | g.35284994C>G | CA405301493 | HAMP | c.207C>G (p.Cys69Trp) n.2478C>G | gnomAD v4 |
19 | g.35284994C>T | CA507041631 | HAMP | c.207C>T (p.Cys69=) n.2478C>T | ClinVar |
19 | g.35284995T>A | CA405301502 | HAMP | c.208T>A (p.Cys70Ser) n.2479T>A | |
19 | g.35284995T>C | CA405301498 | HAMP | c.208T>C (p.Cys70Arg) n.2479T>C | ClinVar dbSNP |
19 | g.35284995T>G | CA405301497 | HAMP | c.208T>G (p.Cys70Gly) n.2479T>G | |
19 | g.35284995T= | CA2333586125 | HAMP | c.208T= (p.Cys70=) n.2479T= | |
19 | g.35284996G>A | CA405301509 | HAMP | c.209G>A (p.Cys70Tyr) n.2480G>A | |
19 | g.35284996G>C | CA405301511 | HAMP | c.209G>C (p.Cys70Ser) n.2480G>C | |
19 | g.35284996G>T | CA405301518 | HAMP | c.209G>T (p.Cys70Phe) n.2480G>T | |
19 | g.35284997C>A | CA405301521 | HAMP | c.210C>A (p.Cys70Ter) n.2481C>A | |
19 | g.35284997C= | CA2333586126 | HAMP | c.210C= (p.Cys70=) n.2481C= | |
19 | g.35284997C>G | CA405301525 | HAMP | c.210C>G (p.Cys70Trp) n.2481C>G | |
19 | g.35284997C>T | CA9375828 | HAMP | c.210C>T (p.Cys70=) n.2481C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.35284998G>A | CA9375829 | HAMP | c.211G>A (p.Gly71Ser) n.2482G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.35284998G>C | CA405301532 | HAMP | c.211G>C (p.Gly71Arg) n.2482G>C | |
19 | g.35284998G= | CA2333586127 | HAMP | c.211G= (p.Gly71=) n.2482G= | |
19 | g.35284998G>T | CA405301535 | HAMP | c.211G>T (p.Gly71Cys) n.2482G>T | gnomAD v4 |
19 | g.35284999G>A | CA340226 | HAMP | c.212G>A (p.Gly71Asp) n.2483G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.35284999G>C | CA405301540 | HAMP | c.212G>C (p.Gly71Ala) n.2483G>C | |
19 | g.35284999G= | CA2333586128 | HAMP | c.212G= (p.Gly71=) n.2483G= | |
19 | g.35284999G>T | CA405301541 | HAMP | c.212G>T (p.Gly71Val) n.2483G>T | |
19 | g.35285000C>A | CA507041652 | HAMP | c.213C>A (p.Gly71=) n.2484C>A | dbSNP gnomAD v2 gnomAD v4 |
19 | g.35285000C= | CA2333586129 | HAMP | c.213C= (p.Gly71=) n.2484C= | |
19 | g.35285000C>G | CA507041654 | HAMP | c.213C>G (p.Gly71=) n.2484C>G | |
19 | g.35285000C>T | CA507041657 | HAMP | c.213C>T (p.Gly71=) n.2484C>T | COSMIC |
19 | g.35285001T>A | CA405301550 | HAMP | c.214T>A (p.Cys72Ser) n.2485T>A | |
19 | g.35285001T>C | CA405301552 | HAMP | c.214T>C (p.Cys72Arg) n.2485T>C | |
19 | g.35285001T>G | CA405301546 | HAMP | c.214T>G (p.Cys72Gly) n.2485T>G | |
19 | g.35285001_35285002delinsTG | CA2333586130 | HAMP | c.214_215delinsTG (p.Cys72=) n.2485_2486delinsTG | |
19 | g.35285002del | CA9375830 | HAMP | c.215del (p.Cys72SerfsTer?) n.2486del | dbSNP ExAC gnomAD v2 |
19 | g.35285002G>A | CA405301557 | HAMP | c.215G>A (p.Cys72Tyr) n.2486G>A | |
19 | g.35285002G>C | CA405301564 | HAMP | c.215G>C (p.Cys72Ser) n.2486G>C | |
19 | g.35285002G>T | CA405301566 | HAMP | c.215G>T (p.Cys72Phe) n.2486G>T | |
19 | g.35285003del | CA405301580 | HAMP | c.216del (p.Cys73ValfsTer?) n.2487del | |
19 | g.35285003C>A | CA333985 | HAMP | c.216C>A (p.Cys72Ter) n.2487C>A | ClinVar dbSNP |
19 | g.35285003C= | CA2333586131 | HAMP | c.216C= (p.Cys72=) n.2487C= | |
19 | g.35285003C>G | CA405301587 | HAMP | c.216C>G (p.Cys72Trp) n.2487C>G | |
19 | g.35285003C>T | CA9375831 | HAMP | c.216C>T (p.Cys72=) n.2487C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.35285004T>A | CA405301590 | HAMP | c.217T>A (p.Cys73Ser) n.2488T>A | |
19 | g.35285004T>C | CA405301593 | HAMP | c.217T>C (p.Cys73Arg) n.2488T>C | |
19 | g.35285004T>G | CA405301596 | HAMP | c.217T>G (p.Cys73Gly) n.2488T>G | |
19 | g.35285005G>A | CA336010 | HAMP | c.218G>A (p.Cys73Tyr) n.2489G>A | ClinVar dbSNP |
19 | g.35285005G>C | CA405301599 | HAMP | c.218G>C (p.Cys73Ser) n.2489G>C | |
19 | g.35285005G= | CA2333586132 | HAMP | c.218G= (p.Cys73=) n.2489G= | |
19 | g.35285005G>T | CA405301605 | HAMP | c.218G>T (p.Cys73Phe) n.2489G>T | |
19 | g.35285006T>A | CA405301607 | HAMP | c.219T>A (p.Cys73Ter) n.2490T>A | |
19 | g.35285006T>C | CA507041701 | HAMP | c.219T>C (p.Cys73=) n.2490T>C | |
19 | g.35285006T>G | CA405301610 | HAMP | c.219T>G (p.Cys73Trp) n.2490T>G | |
19 | g.35285007C>A | CA405301613 | HAMP | c.220C>A (p.His74Asn) n.2491C>A | gnomAD v4 |
19 | g.35285007C>G | CA405301622 | HAMP | c.220C>G (p.His74Asp) n.2491C>G | |
19 | g.35285007C>T | CA405301616 | HAMP | c.220C>T (p.His74Tyr) n.2491C>T | COSMIC |
19 | g.35285008A= | CA2333586133 | HAMP | c.221A= (p.His74=) n.2492A= | |
19 | g.35285008A>C | CA405301629 | HAMP | c.221A>C (p.His74Pro) n.2492A>C | |
19 | g.35285008A>G | CA9375832 | HAMP | c.221A>G (p.His74Arg) n.2492A>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.35285008A>T | CA405301633 | HAMP | c.221A>T (p.His74Leu) n.2492A>T | |
19 | g.35285009T>A | CA405301639 | HAMP | c.222T>A (p.His74Gln) n.2493T>A | |
19 | g.35285009T>C | CA507041708 | HAMP | c.222T>C (p.His74=) n.2493T>C | |
19 | g.35285009T>G | CA405301640 | HAMP | c.222T>G (p.His74Gln) n.2493T>G | |
19 | g.35285010C>A | CA507041711 | HAMP | c.223C>A (p.Arg75=) n.2494C>A | |
19 | g.35285010C= | CA2333586134 | HAMP | c.223C= (p.Arg75=) n.2494C= | |
19 | g.35285010C>G | CA405301644 | HAMP | c.223C>G (p.Arg75Gly) n.2494C>G | ClinVar dbSNP gnomAD v2 gnomAD v4 |
19 | g.35285010C>T | CA9375833 | HAMP | c.223C>T (p.Arg75Ter) n.2494C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.35285011G>A | CA9375834 | HAMP | c.224G>A (p.Arg75Gln) n.2495G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.35285011G>C | CA405301651 | HAMP | c.224G>C (p.Arg75Pro) n.2495G>C | dbSNP gnomAD v3 gnomAD v4 |
19 | g.35285011G= | CA2333586135 | HAMP | c.224G= (p.Arg75=) n.2495G= | |
19 | g.35285011G>T | CA405301654 | HAMP | c.224G>T (p.Arg75Leu) n.2495G>T | |
19 | g.35285012A= | CA2333586136 | HAMP | c.225A= (p.Arg75=) n.2496A= | |
19 | g.35285012A>C | CA507041717 | HAMP | c.225A>C (p.Arg75=) n.2496A>C | |
19 | g.35285012A>G | CA507041723 | HAMP | c.225A>G (p.Arg75=) n.2496A>G | |
19 | g.35285012A>T | CA507041720 | HAMP | c.225A>T (p.Arg75=) n.2496A>T | dbSNP gnomAD v3 gnomAD v4 |
19 | g.35285013T>A | CA405301659 | HAMP | c.226T>A (p.Ser76Thr) n.2497T>A | gnomAD v4 |
19 | g.35285013T>C | CA405301661 | HAMP | c.226T>C (p.Ser76Pro) n.2497T>C | |
19 | g.35285013T>G | CA405301665 | HAMP | c.226T>G (p.Ser76Ala) n.2497T>G | |
19 | g.35285014C>A | CA405301675 | HAMP | c.227C>A (p.Ser76Ter) n.2498C>A | gnomAD v4 |
19 | g.35285014C>G | CA405301672 | HAMP | c.227C>G (p.Ser76Ter) n.2498C>G | |
19 | g.35285014C>T | CA405301669 | HAMP | c.227C>T (p.Ser76Leu) n.2498C>T | |
19 | g.35285015A= | CA2333586137 | HAMP | c.228A= (p.Ser76=) n.2499A= | |
19 | g.35285015A>C | CA507041738 | HAMP | c.228A>C (p.Ser76=) n.2499A>C | ClinVar dbSNP gnomAD v2 gnomAD v4 |
19 | g.35285015A>G | CA507041739 | HAMP | c.228A>G (p.Ser76=) n.2499A>G | |
19 | g.35285015A>T | CA507041740 | HAMP | c.228A>T (p.Ser76=) n.2499A>T | |
19 | g.35285016A>C | CA405301678 | HAMP | c.229A>C (p.Lys77Gln) n.2500A>C | |
19 | g.35285016A>G | CA405301682 | HAMP | c.229A>G (p.Lys77Glu) n.2500A>G | |
19 | g.35285016A>T | CA405301684 | HAMP | c.229A>T (p.Lys77Ter) n.2500A>T | |
19 | g.35285017A>C | CA405301685 | HAMP | c.230A>C (p.Lys77Thr) n.2501A>C | |
19 | g.35285017A>G | CA405301688 | HAMP | c.230A>G (p.Lys77Arg) n.2501A>G | |
19 | g.35285017A>T | CA405301691 | HAMP | c.230A>T (p.Lys77Met) n.2501A>T | |
19 | g.35285018G>A | CA507041750 | HAMP | c.231G>A (p.Lys77=) n.2502G>A | dbSNP |
19 | g.35285018G>C | CA405301693 | HAMP | c.231G>C (p.Lys77Asn) n.2502G>C | |
19 | g.35285018G= | CA2333586138 | HAMP | c.231G= (p.Lys77=) n.2502G= | |
19 | g.35285018G>T | CA405301695 | HAMP | c.231G>T (p.Lys77Asn) n.2502G>T | |
19 | g.35285019T>A | CA405301698 | HAMP | c.232T>A (p.Cys78Ser) n.2503T>A | |
19 | g.35285019T>C | CA405301701 | HAMP | c.232T>C (p.Cys78Arg) n.2503T>C | dbSNP gnomAD v3 gnomAD v4 |
19 | g.35285019T>G | CA405301704 | HAMP | c.232T>G (p.Cys78Gly) n.2503T>G | |
19 | g.35285019T= | CA2333586139 | HAMP | c.232T= (p.Cys78=) n.2503T= | |
19 | g.35285020G>A | CA405301716 | HAMP | c.233G>A (p.Cys78Tyr) n.2504G>A | dbSNP gnomAD v4 |
19 | g.35285020G>C | CA405301717 | HAMP | c.233G>C (p.Cys78Ser) n.2504G>C | |
19 | g.35285020G= | CA2333586140 | HAMP | c.233G= (p.Cys78=) n.2504G= | |
19 | g.35285020G>T | CA405301709 | HAMP | c.233G>T (p.Cys78Phe) n.2504G>T | |
19 | g.35285021T>A | CA405301719 | HAMP | c.234T>A (p.Cys78Ter) n.2505T>A | |
19 | g.35285021T>C | CA507041771 | HAMP | c.234T>C (p.Cys78=) n.2505T>C | |
19 | g.35285021T>G | CA405301720 | HAMP | c.234T>G (p.Cys78Trp) n.2505T>G | |
19 | g.35285022G>A | CA405301723 | HAMP | c.235G>A (p.Gly79Arg) n.2506G>A | |
19 | g.35285022G>C | CA405301725 | HAMP | c.235G>C (p.Gly79Arg) n.2506G>C | |
19 | g.35285022G>T | CA405301738 | HAMP | c.235G>T (p.Gly79Trp) n.2506G>T | |
19 | g.35285023G>A | CA405301747 | HAMP | c.236G>A (p.Gly79Glu) n.2507G>A | |
19 | g.35285023G>C | CA405301745 | HAMP | c.236G>C (p.Gly79Ala) n.2507G>C | |
19 | g.35285023G>T | CA405301742 | HAMP | c.236G>T (p.Gly79Val) n.2507G>T | COSMIC |
19 | g.35285024G>A | CA507041785 | HAMP | c.237G>A (p.Gly79=) n.2508G>A | |
19 | g.35285024G>C | CA507041787 | HAMP | c.237G>C (p.Gly79=) n.2508G>C | |
19 | g.35285024G= | CA2333586141 | HAMP | c.237G= (p.Gly79=) n.2508G= | |
19 | g.35285024G>T | CA507041788 | HAMP | c.237G>T (p.Gly79=) n.2508G>T | dbSNP gnomAD v3 gnomAD v4 |
19 | g.35285025A>C | CA405301752 | HAMP | c.238A>C (p.Met80Leu) n.2509A>C | |
19 | g.35285025A>G | CA405301754 | HAMP | c.238A>G (p.Met80Val) n.2509A>G | gnomAD v4 |
19 | g.35285025A>T | CA405301758 | HAMP | c.238A>T (p.Met80Leu) n.2509A>T | gnomAD v4 |
19 | g.35285026T>A | CA405301762 | HAMP | c.239T>A (p.Met80Lys) n.2510T>A | |
19 | g.35285026T>C | CA405301764 | HAMP | c.239T>C (p.Met80Thr) n.2510T>C | |
19 | g.35285026T>G | CA405301766 | HAMP | c.239T>G (p.Met80Arg) n.2510T>G | |
19 | g.35285027G>A | CA405301769 | HAMP | c.240G>A (p.Met80Ile) n.2511G>A | |
19 | g.35285027G>C | CA405301775 | HAMP | c.240G>C (p.Met80Ile) n.2511G>C | |
19 | g.35285027G>T | CA405301772 | HAMP | c.240G>T (p.Met80Ile) n.2511G>T | |
19 | g.35285028T>A | CA405301778 | HAMP | c.241T>A (p.Cys81Ser) n.2512T>A | |
19 | g.35285028T>C | CA405301780 | HAMP | c.241T>C (p.Cys81Arg) n.2512T>C | |
19 | g.35285028T>G | CA405301783 | HAMP | c.241T>G (p.Cys81Gly) n.2512T>G | |
19 | g.35285029G>A | CA405301787 | HAMP | c.242G>A (p.Cys81Tyr) n.2513G>A | COSMIC |
19 | g.35285029G>C | CA405301790 | HAMP | c.242G>C (p.Cys81Ser) n.2513G>C | gnomAD v4 |
19 | g.35285029G>T | CA405301795 | HAMP | c.242G>T (p.Cys81Phe) n.2513G>T | |
19 | g.35285030C>A | CA405301796 | HAMP | c.243C>A (p.Cys81Ter) n.2514C>A | gnomAD v4 |
19 | g.35285030C>G | CA405301798 | HAMP | c.243C>G (p.Cys81Trp) n.2514C>G | |
19 | g.35285030C>T | CA507041801 | HAMP | c.243C>T (p.Cys81=) n.2514C>T | |
19 | g.35285031T>A | CA405301802 | HAMP | c.244T>A (p.Cys82Ser) n.2515T>A | |
19 | g.35285031T>C | CA405301803 | HAMP | c.244T>C (p.Cys82Arg) n.2515T>C | |
19 | g.35285031T>G | CA405301804 | HAMP | c.244T>G (p.Cys82Gly) n.2515T>G | |
19 | g.35285032G>A | CA405301813 | HAMP | c.245G>A (p.Cys82Tyr) n.2516G>A | gnomAD v4 |
19 | g.35285032G>C | CA405301810 | HAMP | c.245G>C (p.Cys82Ser) n.2516G>C | |
19 | g.35285032G>T | CA405301807 | HAMP | c.245G>T (p.Cys82Phe) n.2516G>T | gnomAD v4 |
19 | g.35285033C>A | CA405301816 | HAMP | c.246C>A (p.Cys82Ter) n.2517C>A | gnomAD v4 |
19 | g.35285033C>G | CA405301817 | HAMP | c.246C>G (p.Cys82Trp) n.2517C>G | |
19 | g.35285033C>T | CA507041806 | HAMP | c.246C>T (p.Cys82=) n.2517C>T | gnomAD v4 |
19 | g.35285034A>C | CA405301820 | HAMP | c.247A>C (p.Lys83Gln) n.2518A>C | |
19 | g.35285034A>G | CA405301823 | HAMP | c.247A>G (p.Lys83Glu) n.2518A>G | |
19 | g.35285034A>T | CA405301825 | HAMP | c.247A>T (p.Lys83Ter) n.2518A>T | |
19 | g.35285035A= | CA2333586142 | HAMP | c.248A= (p.Lys83=) n.2519A= | |
19 | g.35285035A>C | CA405301826 | HAMP | c.248A>C (p.Lys83Thr) n.2519A>C | |
19 | g.35285035A>G | CA9375835 | HAMP | c.248A>G (p.Lys83Arg) n.2519A>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.35285035A>T | CA405301830 | HAMP | c.248A>T (p.Lys83Met) n.2519A>T | |
19 | g.35285036G>A | CA507041811 | HAMP | c.249G>A (p.Lys83=) n.2520G>A | |
19 | g.35285036G>C | CA405301833 | HAMP | c.249G>C (p.Lys83Asn) n.2520G>C | gnomAD v4 |
19 | g.35285036G>T | CA405301836 | HAMP | c.249G>T (p.Lys83Asn) n.2520G>T |