Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.13753776T>A | CA384054397 | GRIN2B | c.551A>T (p.Asn184Ile) | |
12 | g.13753776T>C | CA384054398 | GRIN2B | c.551A>G (p.Asn184Ser) | |
12 | g.13753776T>G | CA384054399 | GRIN2B | c.551A>C (p.Asn184Thr) | |
12 | g.13753777T>A | CA384054401 | GRIN2B | c.550A>T (p.Asn184Tyr) | |
12 | g.13753777T>C | CA384054403 | GRIN2B | c.550A>G (p.Asn184Asp) | |
12 | g.13753777T>G | CA384054400 | GRIN2B | c.550A>C (p.Asn184His) | |
12 | g.13753778T>A | CA478853827 | GRIN2B | c.549A>T (p.Val183=) | |
12 | g.13753778T>C | CA478853828 | GRIN2B | c.549A>G (p.Val183=) | |
12 | g.13753778T>G | CA478853829 | GRIN2B | c.549A>C (p.Val183=) | |
12 | g.13753779A>C | CA384054405 | GRIN2B | c.548T>G (p.Val183Gly) | |
12 | g.13753779A>G | CA384054412 | GRIN2B | c.548T>C (p.Val183Ala) | |
12 | g.13753779A>T | CA384054413 | GRIN2B | c.548T>A (p.Val183Glu) | |
12 | g.13753780C>A | CA384054415 | GRIN2B | c.547G>T (p.Val183Leu) | |
12 | g.13753780C>G | CA384054416 | GRIN2B | c.547G>C (p.Val183Leu) | |
12 | g.13753780C>T | CA384054417 | GRIN2B | c.547G>A (p.Val183Ile) | |
12 | g.13753781A= | CA2017525956 | GRIN2B | c.546T= (p.Phe182=) | |
12 | g.13753781A>C | CA384054419 | GRIN2B | c.546T>G (p.Phe182Leu) | |
12 | g.13753781A>G | CA6461386 | GRIN2B | c.546T>C (p.Phe182=) | dbSNP ExAC |
12 | g.13753781A>T | CA384054421 | GRIN2B | c.546T>A (p.Phe182Leu) | |
12 | g.13753782A>C | CA384054422 | GRIN2B | c.545T>G (p.Phe182Cys) | |
12 | g.13753782A>G | CA384054423 | GRIN2B | c.545T>C (p.Phe182Ser) | |
12 | g.13753782A>T | CA384054425 | GRIN2B | c.545T>A (p.Phe182Tyr) | |
12 | g.13753783A>C | CA384054430 | GRIN2B | c.544T>G (p.Phe182Val) | ClinVar |
12 | g.13753783A>G | CA384054426 | GRIN2B | c.544T>C (p.Phe182Leu) | ClinVar gnomAD v4 |
12 | g.13753783A>T | CA384054428 | GRIN2B | c.544T>A (p.Phe182Ile) | |
12 | g.13753784G>A | CA478853830 | GRIN2B | c.543C>T (p.Asp181=) | |
12 | g.13753784G>C | CA384054431 | GRIN2B | c.543C>G (p.Asp181Glu) | |
12 | g.13753784G>T | CA384054432 | GRIN2B | c.543C>A (p.Asp181Glu) | |
12 | g.13753785T>A | CA384054434 | GRIN2B | c.542A>T (p.Asp181Val) | |
12 | g.13753785T>C | CA16613688 | GRIN2B | c.542A>G (p.Asp181Gly) | ClinVar dbSNP |
12 | g.13753785T>G | CA384054435 | GRIN2B | c.542A>C (p.Asp181Ala) | |
12 | g.13753785T= | CA2017525957 | GRIN2B | c.542A= (p.Asp181=) | |
12 | g.13753786C>A | CA384054437 | GRIN2B | c.541G>T (p.Asp181Tyr) | |
12 | g.13753786C>G | CA384054438 | GRIN2B | c.541G>C (p.Asp181His) | |
12 | g.13753786C>T | CA384054440 | GRIN2B | c.541G>A (p.Asp181Asn) | COSMIC |
12 | g.13753787C>A | CA384054442 | GRIN2B | c.540G>T (p.Gln180His) | |
12 | g.13753787C= | CA2017525958 | GRIN2B | c.540G= (p.Gln180=) | |
12 | g.13753787C>G | CA384054444 | GRIN2B | c.540G>C (p.Gln180His) | |
12 | g.13753787C>T | CA16606563 | GRIN2B | c.540G>A (p.Gln180=) | ClinVar dbSNP gnomAD v4 COSMIC |
12 | g.13753788T>A | CA384054450 | GRIN2B | c.539A>T (p.Gln180Leu) | |
12 | g.13753788T>C | CA384054448 | GRIN2B | c.539A>G (p.Gln180Arg) | gnomAD v4 |
12 | g.13753788T>G | CA384054447 | GRIN2B | c.539A>C (p.Gln180Pro) | dbSNP gnomAD v2 gnomAD v4 |
12 | g.13753788T= | CA2017525959 | GRIN2B | c.539A= (p.Gln180=) | |
12 | g.13753789G>A | CA384054452 | GRIN2B | c.538C>T (p.Gln180Ter) | ClinVar dbSNP |
12 | g.13753789G>C | CA384054455 | GRIN2B | c.538C>G (p.Gln180Glu) | |
12 | g.13753789G= | CA2017525960 | GRIN2B | c.538C= (p.Gln180=) | |
12 | g.13753789G>T | CA384054453 | GRIN2B | c.538C>A (p.Gln180Lys) | |
12 | g.13753790G>A | CA478853831 | GRIN2B | c.537C>T (p.Tyr179=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
12 | g.13753790G>C | CA384054456 | GRIN2B | c.537C>G (p.Tyr179Ter) | |
12 | g.13753790G= | CA2017525961 | GRIN2B | c.537C= (p.Tyr179=) | |
12 | g.13753790G>T | CA384054458 | GRIN2B | c.537C>A (p.Tyr179Ter) | dbSNP |
12 | g.13753791T>A | CA384054461 | GRIN2B | c.536A>T (p.Tyr179Phe) | |
12 | g.13753791T>C | CA384054463 | GRIN2B | c.536A>G (p.Tyr179Cys) | |
12 | g.13753791T>G | CA384054464 | GRIN2B | c.536A>C (p.Tyr179Ser) | |
12 | g.13753792A= | CA2017525962 | GRIN2B | c.535T= (p.Tyr179=) | |
12 | g.13753792A>C | CA384054468 | GRIN2B | c.535T>G (p.Tyr179Asp) | |
12 | g.13753792A>G | CA384054466 | GRIN2B | c.535T>C (p.Tyr179His) | dbSNP gnomAD v2 gnomAD v4 |
12 | g.13753792A>T | CA384054465 | GRIN2B | c.535T>A (p.Tyr179Asn) | |
12 | g.13753793G>A | CA478853832 | GRIN2B | c.534C>T (p.Gly178=) | |
12 | g.13753793G>C | CA478853833 | GRIN2B | c.534C>G (p.Gly178=) | |
12 | g.13753793G= | CA2017525963 | GRIN2B | c.534C= (p.Gly178=) | |
12 | g.13753793G>T | CA478853834 | GRIN2B | c.534C>A (p.Gly178=) | dbSNP gnomAD v2 |
12 | g.13753794C>A | CA384054469 | GRIN2B | c.533G>T (p.Gly178Val) | |
12 | g.13753794C>G | CA384054470 | GRIN2B | c.533G>C (p.Gly178Ala) | |
12 | g.13753794C>T | CA384054472 | GRIN2B | c.533G>A (p.Gly178Asp) | ClinVar gnomAD v4 |
12 | g.13753795del | CA2575085881 | GRIN2B | c.533del (p.Gly178AlafsTer6) | |
12 | g.13753795C>A | CA384054474 | GRIN2B | c.532G>T (p.Gly178Cys) | |
12 | g.13753795C>G | CA384054476 | GRIN2B | c.532G>C (p.Gly178Arg) | |
12 | g.13753795C>T | CA384054477 | GRIN2B | c.532G>A (p.Gly178Ser) | |
12 | g.13753796A>C | CA478853835 | GRIN2B | c.531T>G (p.Pro177=) | |
12 | g.13753796A>G | CA478853836 | GRIN2B | c.531T>C (p.Pro177=) | |
12 | g.13753796A>T | CA478853837 | GRIN2B | c.531T>A (p.Pro177=) | |
12 | g.13753797G>A | CA384054483 | GRIN2B | c.530C>T (p.Pro177Leu) | COSMIC |
12 | g.13753797G>C | CA384054479 | GRIN2B | c.530C>G (p.Pro177Arg) | |
12 | g.13753797G>T | CA384054481 | GRIN2B | c.530C>A (p.Pro177His) | COSMIC |
12 | g.13753798G>A | CA6461387 | GRIN2B | c.529C>T (p.Pro177Ser) | dbSNP ExAC gnomAD v2 gnomAD v4 |
12 | g.13753798G>C | CA384054485 | GRIN2B | c.529C>G (p.Pro177Ala) | |
12 | g.13753798G= | CA2017525964 | GRIN2B | c.529C= (p.Pro177=) | |
12 | g.13753798G>T | CA384054487 | GRIN2B | c.529C>A (p.Pro177Thr) | COSMIC |
12 | g.13753799G>A | CA478853838 | GRIN2B | c.528C>T (p.Phe176=) | COSMIC |
12 | g.13753799G>C | CA384054488 | GRIN2B | c.528C>G (p.Phe176Leu) | |
12 | g.13753799G>T | CA384054490 | GRIN2B | c.528C>A (p.Phe176Leu) | |
12 | g.13753800A>C | CA384054492 | GRIN2B | c.527T>G (p.Phe176Cys) | |
12 | g.13753800A>G | CA384054493 | GRIN2B | c.527T>C (p.Phe176Ser) | |
12 | g.13753800A>T | CA384054497 | GRIN2B | c.527T>A (p.Phe176Tyr) | |
12 | g.13753801A>C | CA384054499 | GRIN2B | c.526T>G (p.Phe176Val) | |
12 | g.13753801A>G | CA384054501 | GRIN2B | c.526T>C (p.Phe176Leu) | |
12 | g.13753801A>T | CA384054503 | GRIN2B | c.526T>A (p.Phe176Ile) | |
12 | g.13753802A>C | CA384054505 | GRIN2B | c.525T>G (p.Tyr175Ter) | |
12 | g.13753802A>G | CA478853839 | GRIN2B | c.525T>C (p.Tyr175=) | gnomAD v4 |
12 | g.13753802A>T | CA384054507 | GRIN2B | c.525T>A (p.Tyr175Ter) | |
12 | g.13753803T>A | CA384054513 | GRIN2B | c.524A>T (p.Tyr175Phe) | |
12 | g.13753803T>C | CA384054509 | GRIN2B | c.524A>G (p.Tyr175Cys) | |
12 | g.13753803T>G | CA384054511 | GRIN2B | c.524A>C (p.Tyr175Ser) | |
12 | g.13753804A>C | CA384054517 | GRIN2B | c.523T>G (p.Tyr175Asp) | |
12 | g.13753804A>G | CA384054518 | GRIN2B | c.523T>C (p.Tyr175His) | |
12 | g.13753804A>T | CA384054521 | GRIN2B | c.523T>A (p.Tyr175Asn) | |
12 | g.13753805G>A | CA478853840 | GRIN2B | c.522C>T (p.Thr174=) | |
12 | g.13753805G>C | CA478853841 | GRIN2B | c.522C>G (p.Thr174=) | |
12 | g.13753805G>T | CA478853842 | GRIN2B | c.522C>A (p.Thr174=) | |
12 | g.13753806G>A | CA384054523 | GRIN2B | c.521C>T (p.Thr174Ile) | |
12 | g.13753806G>C | CA384054525 | GRIN2B | c.521C>G (p.Thr174Ser) | |
12 | g.13753806G>T | CA384054527 | GRIN2B | c.521C>A (p.Thr174Asn) | |
12 | g.13753807T>A | CA384054532 | GRIN2B | c.520A>T (p.Thr174Ser) | |
12 | g.13753807T>C | CA384054529 | GRIN2B | c.520A>G (p.Thr174Ala) | |
12 | g.13753807T>G | CA384054531 | GRIN2B | c.520A>C (p.Thr174Pro) | |
12 | g.13753808G>A | CA6461389 | GRIN2B | c.519C>T (p.Thr173=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
12 | g.13753808G>C | CA6461388 | GRIN2B | c.519C>G (p.Thr173=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.13753808G= | CA2017525965 | GRIN2B | c.519C= (p.Thr173=) | |
12 | g.13753808G>T | CA478853843 | GRIN2B | c.519C>A (p.Thr173=) | |
12 | g.13753809G>A | CA384054536 | GRIN2B | c.518C>T (p.Thr173Ile) | gnomAD v4 COSMIC |
12 | g.13753809G>C | CA384054537 | GRIN2B | c.518C>G (p.Thr173Ser) | |
12 | g.13753809G>T | CA384054538 | GRIN2B | c.518C>A (p.Thr173Asn) | |
12 | g.13753810T>A | CA384054540 | GRIN2B | c.517A>T (p.Thr173Ser) | |
12 | g.13753810T>C | CA384054545 | GRIN2B | c.517A>G (p.Thr173Ala) | |
12 | g.13753810T>G | CA384054543 | GRIN2B | c.517A>C (p.Thr173Pro) | |
12 | g.13753811G>A | CA478853844 | GRIN2B | c.516C>T (p.Val172=) | dbSNP gnomAD v2 gnomAD v4 |
12 | g.13753811G>C | CA478853846 | GRIN2B | c.516C>G (p.Val172=) | |
12 | g.13753811G= | CA2017525966 | GRIN2B | c.516C= (p.Val172=) | |
12 | g.13753811G>T | CA478853845 | GRIN2B | c.516C>A (p.Val172=) | |
12 | g.13753812A>C | CA384054546 | GRIN2B | c.515T>G (p.Val172Gly) | |
12 | g.13753812A>G | CA384054547 | GRIN2B | c.515T>C (p.Val172Ala) | |
12 | g.13753812A>T | CA384054549 | GRIN2B | c.515T>A (p.Val172Asp) | |
12 | g.13753813C>A | CA384054550 | GRIN2B | c.514G>T (p.Val172Phe) | |
12 | g.13753813C= | CA2017525967 | GRIN2B | c.514G= (p.Val172=) | |
12 | g.13753813C>G | CA384054551 | GRIN2B | c.514G>C (p.Val172Leu) | |
12 | g.13753813C>T | CA6461390 | GRIN2B | c.514G>A (p.Val172Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
12 | g.13753814G>A | CA6461391 | GRIN2B | c.513C>T (p.Ile171=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
12 | g.13753814G>C | CA384054553 | GRIN2B | c.513C>G (p.Ile171Met) | gnomAD v4 |
12 | g.13753814G= | CA2017525968 | GRIN2B | c.513C= (p.Ile171=) | |
12 | g.13753814G>T | CA478853847 | GRIN2B | c.513C>A (p.Ile171=) | dbSNP gnomAD v2 gnomAD v4 |
12 | g.13753815A>C | CA384054555 | GRIN2B | c.512T>G (p.Ile171Ser) | |
12 | g.13753815A>G | CA384054557 | GRIN2B | c.512T>C (p.Ile171Thr) | |
12 | g.13753815A>T | CA384054558 | GRIN2B | c.512T>A (p.Ile171Asn) | ClinVar |
12 | g.13753816T>A | CA384054561 | GRIN2B | c.511A>T (p.Ile171Phe) | ClinVar |
12 | g.13753816T>C | CA384054559 | GRIN2B | c.511A>G (p.Ile171Val) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
12 | g.13753816T>G | CA384054560 | GRIN2B | c.511A>C (p.Ile171Leu) | |
12 | g.13753816T= | CA2017525969 | GRIN2B | c.511A= (p.Ile171=) | |
12 | g.13753817A= | CA2017525970 | GRIN2B | c.510T= (p.Ser170=) | |
12 | g.13753817A>C | CA478853848 | GRIN2B | c.510T>G (p.Ser170=) | gnomAD v4 |
12 | g.13753817A>G | CA6461392 | GRIN2B | c.510T>C (p.Ser170=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
12 | g.13753817A>T | CA478853849 | GRIN2B | c.510T>A (p.Ser170=) | |
12 | g.13753818G>A | CA384054563 | GRIN2B | c.509C>T (p.Ser170Phe) | ClinVar COSMIC |
12 | g.13753818G>C | CA384054565 | GRIN2B | c.509C>G (p.Ser170Cys) | |
12 | g.13753818G>T | CA384054567 | GRIN2B | c.509C>A (p.Ser170Tyr) | COSMIC |
12 | g.13753819A>C | CA384054568 | GRIN2B | c.508T>G (p.Ser170Ala) | |
12 | g.13753819A>G | CA384054569 | GRIN2B | c.508T>C (p.Ser170Pro) | |
12 | g.13753819A>T | CA384054570 | GRIN2B | c.508T>A (p.Ser170Thr) | |
12 | g.13753820A>C | CA384054571 | GRIN2B | c.507T>G (p.Phe169Leu) | |
12 | g.13753820A>G | CA478853850 | GRIN2B | c.507T>C (p.Phe169=) | |
12 | g.13753820A>T | CA384054573 | GRIN2B | c.507T>A (p.Phe169Leu) | |
12 | g.13753821A>C | CA384054574 | GRIN2B | c.506T>G (p.Phe169Cys) | |
12 | g.13753821A>G | CA384054576 | GRIN2B | c.506T>C (p.Phe169Ser) | |
12 | g.13753821A>T | CA384054577 | GRIN2B | c.506T>A (p.Phe169Tyr) | |
12 | g.13753822A>C | CA384054578 | GRIN2B | c.505T>G (p.Phe169Val) | |
12 | g.13753822A>G | CA384054580 | GRIN2B | c.505T>C (p.Phe169Leu) | |
12 | g.13753822A>T | CA384054582 | GRIN2B | c.505T>A (p.Phe169Ile) | |
12 | g.13753823G>A | CA478853851 | GRIN2B | c.504C>T (p.Ile168=) | |
12 | g.13753823G>C | CA384054584 | GRIN2B | c.504C>G (p.Ile168Met) | |
12 | g.13753823G= | CA2017525971 | GRIN2B | c.504C= (p.Ile168=) | |
12 | g.13753823G>T | CA288906 | GRIN2B | c.504C>A (p.Ile168=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.13753824A= | CA2017525972 | GRIN2B | c.503T= (p.Ile168=) | |
12 | g.13753824A>C | CA384054587 | GRIN2B | c.503T>G (p.Ile168Ser) | |
12 | g.13753824A>G | CA6461393 | GRIN2B | c.503T>C (p.Ile168Thr) | dbSNP ExAC gnomAD v2 gnomAD v4 |
12 | g.13753824A>T | CA384054589 | GRIN2B | c.503T>A (p.Ile168Asn) | |
12 | g.13753825T>A | CA384054591 | GRIN2B | c.502A>T (p.Ile168Phe) | |
12 | g.13753825T>C | CA384054593 | GRIN2B | c.502A>G (p.Ile168Val) | dbSNP gnomAD v4 |
12 | g.13753825T>G | CA384054594 | GRIN2B | c.502A>C (p.Ile168Leu) | |
12 | g.13753825T= | CA2017525973 | GRIN2B | c.502A= (p.Ile168=) | |
12 | g.13753826G>A | CA6461394 | GRIN2B | c.501C>T (p.Tyr167=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
12 | g.13753826G>C | CA384054595 | GRIN2B | c.501C>G (p.Tyr167Ter) | |
12 | g.13753826G= | CA2017525974 | GRIN2B | c.501C= (p.Tyr167=) | |
12 | g.13753826G>T | CA384054597 | GRIN2B | c.501C>A (p.Tyr167Ter) | |
12 | g.13753827T>A | CA384054599 | GRIN2B | c.500A>T (p.Tyr167Phe) | |
12 | g.13753827T>C | CA384054600 | GRIN2B | c.500A>G (p.Tyr167Cys) | |
12 | g.13753827T>G | CA384054601 | GRIN2B | c.500A>C (p.Tyr167Ser) | |
12 | g.13753828A= | CA2017525975 | GRIN2B | c.499T= (p.Tyr167=) | |
12 | g.13753828A>C | CA384054606 | GRIN2B | c.499T>G (p.Tyr167Asp) | dbSNP |
12 | g.13753828A>G | CA384054603 | GRIN2B | c.499T>C (p.Tyr167His) | |
12 | g.13753828A>T | CA384054605 | GRIN2B | c.499T>A (p.Tyr167Asn) | |
12 | g.13753829C>A | CA384054609 | GRIN2B | c.498G>T (p.Trp166Cys) | dbSNP |
12 | g.13753829C= | CA2017525976 | GRIN2B | c.498G= (p.Trp166=) | |
12 | g.13753829C>G | CA384054610 | GRIN2B | c.498G>C (p.Trp166Cys) | |
12 | g.13753829C>T | CA384054612 | GRIN2B | c.498G>A (p.Trp166Ter) | dbSNP |
12 | g.13753830C>A | CA384054613 | GRIN2B | c.497G>T (p.Trp166Leu) | |
12 | g.13753830C= | CA2017525977 | GRIN2B | c.497G= (p.Trp166=) | |
12 | g.13753830C>G | CA384054615 | GRIN2B | c.497G>C (p.Trp166Ser) | |
12 | g.13753830C>T | CA384054617 | GRIN2B | c.497G>A (p.Trp166Ter) | dbSNP |
12 | g.13753831A>C | CA384054619 | GRIN2B | c.496T>G (p.Trp166Gly) | |
12 | g.13753831A>G | CA384054623 | GRIN2B | c.496T>C (p.Trp166Arg) | |
12 | g.13753831A>T | CA384054624 | GRIN2B | c.496T>A (p.Trp166Arg) | gnomAD v4 |
12 | g.13753832G>A | CA6461395 | GRIN2B | c.495C>T (p.Asp165=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
12 | g.13753832G>C | CA384054627 | GRIN2B | c.495C>G (p.Asp165Glu) | |
12 | g.13753832G= | CA2017525978 | GRIN2B | c.495C= (p.Asp165=) | |
12 | g.13753832G>T | CA384054628 | GRIN2B | c.495C>A (p.Asp165Glu) | |
12 | g.13753833T>A | CA384054634 | GRIN2B | c.494A>T (p.Asp165Val) | |
12 | g.13753833T>C | CA384054633 | GRIN2B | c.494A>G (p.Asp165Gly) | |
12 | g.13753833T>G | CA384054631 | GRIN2B | c.494A>C (p.Asp165Ala) | |
12 | g.13753834C>A | CA384054635 | GRIN2B | c.493G>T (p.Asp165Tyr) | |
12 | g.13753834C>G | CA384054637 | GRIN2B | c.493G>C (p.Asp165His) | |
12 | g.13753834C>T | CA384054639 | GRIN2B | c.493G>A (p.Asp165Asn) | |
12 | g.13753835A>C | CA384054640 | GRIN2B | c.492T>G (p.Tyr164Ter) | |
12 | g.13753835A>G | CA478853852 | GRIN2B | c.492T>C (p.Tyr164=) | |
12 | g.13753835A>T | CA384054642 | GRIN2B | c.492T>A (p.Tyr164Ter) | |
12 | g.13753836T>A | CA384054644 | GRIN2B | c.491A>T (p.Tyr164Phe) | |
12 | g.13753836T>C | CA384054646 | GRIN2B | c.491A>G (p.Tyr164Cys) | |
12 | g.13753836T>G | CA384054648 | GRIN2B | c.491A>C (p.Tyr164Ser) | |
12 | g.13753837A>C | CA384054649 | GRIN2B | c.490T>G (p.Tyr164Asp) | |
12 | g.13753837A>G | CA384054651 | GRIN2B | c.490T>C (p.Tyr164His) | |
12 | g.13753837A>T | CA384054653 | GRIN2B | c.490T>A (p.Tyr164Asn) | |
12 | g.13753838T>A | CA384054654 | GRIN2B | c.489A>T (p.Glu163Asp) | |
12 | g.13753838T>C | CA478853853 | GRIN2B | c.489A>G (p.Glu163=) | |
12 | g.13753838T>G | CA384054656 | GRIN2B | c.489A>C (p.Glu163Asp) | |
12 | g.13753839T>A | CA384054659 | GRIN2B | c.488A>T (p.Glu163Val) | |
12 | g.13753839T>C | CA384054660 | GRIN2B | c.488A>G (p.Glu163Gly) | |
12 | g.13753839T>G | CA384054658 | GRIN2B | c.488A>C (p.Glu163Ala) | |
12 | g.13753840C>A | CA384054661 | GRIN2B | c.487G>T (p.Glu163Ter) | dbSNP |
12 | g.13753840C= | CA2017525979 | GRIN2B | c.487G= (p.Glu163=) | |
12 | g.13753840C>G | CA384054664 | GRIN2B | c.487G>C (p.Glu163Gln) | |
12 | g.13753840C>T | CA384054662 | GRIN2B | c.487G>A (p.Glu163Lys) | |
12 | g.13753841T>A | CA384054666 | GRIN2B | c.486A>T (p.Glu162Asp) | |
12 | g.13753841T>C | CA478853505 | GRIN2B | c.486A>G (p.Glu162=) | |
12 | g.13753841T>G | CA384054667 | GRIN2B | c.486A>C (p.Glu162Asp) | |
12 | g.13753842T>A | CA384054669 | GRIN2B | c.485A>T (p.Glu162Val) | |
12 | g.13753842T>C | CA384054671 | GRIN2B | c.485A>G (p.Glu162Gly) | |
12 | g.13753842T>G | CA384054673 | GRIN2B | c.485A>C (p.Glu162Ala) | |
12 | g.13753843C>A | CA384054675 | GRIN2B | c.484G>T (p.Glu162Ter) | dbSNP COSMIC |
12 | g.13753843C= | CA2017525980 | GRIN2B | c.484G= (p.Glu162=) | |
12 | g.13753843C>G | CA384054676 | GRIN2B | c.484G>C (p.Glu162Gln) | |
12 | g.13753843C>T | CA384054678 | GRIN2B | c.484G>A (p.Glu162Lys) | |
12 | g.13753843_13753844insTTTA | CA603495915 | GRIN2B | c.483_484insTAAA (p.Glu162Ter) | dbSNP gnomAD v2 |
12 | g.13753844C>A | CA384054679 | GRIN2B | c.483G>T (p.Met161Ile) | |
12 | g.13753844C>G | CA384054680 | GRIN2B | c.483G>C (p.Met161Ile) | |
12 | g.13753844C>T | CA384054682 | GRIN2B | c.483G>A (p.Met161Ile) | |
12 | g.13753844_13753848delinsCATGA | CA2017525981 | GRIN2B | c.479_483delinsTCATG (p.Ile160=) | |
12 | g.13753845A>C | CA384054687 | GRIN2B | c.482T>G (p.Met161Arg) | |
12 | g.13753845A>G | CA384054686 | GRIN2B | c.482T>C (p.Met161Thr) | |
12 | g.13753845A>T | CA384054684 | GRIN2B | c.482T>A (p.Met161Lys) | |
12 | g.13753845_13753848del | CA603495916 | GRIN2B | c.479_482del (p.Ile160ArgfsTer23) | dbSNP gnomAD v2 |
12 | g.13753846T>A | CA384054689 | GRIN2B | c.481A>T (p.Met161Leu) | |
12 | g.13753846T>C | CA384054691 | GRIN2B | c.481A>G (p.Met161Val) | |
12 | g.13753846T>G | CA384054693 | GRIN2B | c.481A>C (p.Met161Leu) | |
12 | g.13753847G>A | CA478853512 | GRIN2B | c.480C>T (p.Ile160=) | gnomAD v4 COSMIC |
12 | g.13753847G>C | CA384054694 | GRIN2B | c.480C>G (p.Ile160Met) | |
12 | g.13753847G>T | CA478853513 | GRIN2B | c.480C>A (p.Ile160=) | COSMIC |
12 | g.13753848A>C | CA384054696 | GRIN2B | c.479T>G (p.Ile160Ser) | |
12 | g.13753848A>G | CA384054697 | GRIN2B | c.479T>C (p.Ile160Thr) | COSMIC |
12 | g.13753848A>T | CA384054699 | GRIN2B | c.479T>A (p.Ile160Asn) | |
12 | g.13753849T>A | CA384054702 | GRIN2B | c.478A>T (p.Ile160Phe) | ClinVar gnomAD v4 |
12 | g.13753849T>C | CA384054704 | GRIN2B | c.478A>G (p.Ile160Val) | |
12 | g.13753849T>G | CA384054705 | GRIN2B | c.478A>C (p.Ile160Leu) | |
12 | g.13753850G>A | CA478853515 | GRIN2B | c.477C>T (p.Asn159=) | |
12 | g.13753850G>C | CA384054707 | GRIN2B | c.477C>G (p.Asn159Lys) | |
12 | g.13753850G>T | CA384054709 | GRIN2B | c.477C>A (p.Asn159Lys) | |
12 | g.13753851T>A | CA384054715 | GRIN2B | c.476A>T (p.Asn159Ile) | |
12 | g.13753851T>C | CA384054711 | GRIN2B | c.476A>G (p.Asn159Ser) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
12 | g.13753851T>G | CA384054710 | GRIN2B | c.476A>C (p.Asn159Thr) | |
12 | g.13753851T= | CA2017525982 | GRIN2B | c.476A= (p.Asn159=) | |
12 | g.13753852T>A | CA384054720 | GRIN2B | c.475A>T (p.Asn159Tyr) | |
12 | g.13753852T>C | CA384054717 | GRIN2B | c.475A>G (p.Asn159Asp) | |
12 | g.13753852T>G | CA384054719 | GRIN2B | c.475A>C (p.Asn159His) | |
12 | g.13753853G>A | CA478853517 | GRIN2B | c.474C>T (p.Leu158=) | |
12 | g.13753853G>C | CA478853518 | GRIN2B | c.474C>G (p.Leu158=) | dbSNP |
12 | g.13753853G= | CA2017525983 | GRIN2B | c.474C= (p.Leu158=) | |
12 | g.13753853G>T | CA478853519 | GRIN2B | c.474C>A (p.Leu158=) | gnomAD v4 |
12 | g.13753854A>C | CA384054722 | GRIN2B | c.473T>G (p.Leu158Arg) | |
12 | g.13753854A>G | CA384054723 | GRIN2B | c.473T>C (p.Leu158Pro) | |
12 | g.13753854A>T | CA384054725 | GRIN2B | c.473T>A (p.Leu158His) | |
12 | g.13753855G>A | CA6461396 | GRIN2B | c.472C>T (p.Leu158Phe) | dbSNP ExAC gnomAD v2 gnomAD v4 |
12 | g.13753855G>C | CA384054729 | GRIN2B | c.472C>G (p.Leu158Val) | |
12 | g.13753855G= | CA2017525984 | GRIN2B | c.472C= (p.Leu158=) | |
12 | g.13753855G>T | CA384054727 | GRIN2B | c.472C>A (p.Leu158Ile) | |
12 | g.13753856C>A | CA384054731 | GRIN2B | c.471G>T (p.Met157Ile) | |
12 | g.13753856C= | CA2017525985 | GRIN2B | c.471G= (p.Met157=) | |
12 | g.13753856C>G | CA10577451 | GRIN2B | c.471G>C (p.Met157Ile) | ClinVar dbSNP |
12 | g.13753856C>T | CA384054733 | GRIN2B | c.471G>A (p.Met157Ile) | |
12 | g.13753857A>C | CA384054736 | GRIN2B | c.470T>G (p.Met157Arg) | |
12 | g.13753857A>G | CA384054738 | GRIN2B | c.470T>C (p.Met157Thr) | |
12 | g.13753857A>T | CA384054740 | GRIN2B | c.470T>A (p.Met157Lys) | |
12 | g.13753858T>A | CA384054741 | GRIN2B | c.469A>T (p.Met157Leu) | |
12 | g.13753858T>C | CA384054744 | GRIN2B | c.469A>G (p.Met157Val) | gnomAD v4 |
12 | g.13753858T>G | CA384054743 | GRIN2B | c.469A>C (p.Met157Leu) | |
12 | g.13753859T>A | CA478853520 | GRIN2B | c.468A>T (p.Val156=) | |
12 | g.13753859T>C | CA478853522 | GRIN2B | c.468A>G (p.Val156=) | |
12 | g.13753859T>G | CA478853521 | GRIN2B | c.468A>C (p.Val156=) | |
12 | g.13753860A>C | CA384054746 | GRIN2B | c.467T>G (p.Val156Gly) | |
12 | g.13753860A>G | CA384054748 | GRIN2B | c.467T>C (p.Val156Ala) | |
12 | g.13753860A>T | CA384054750 | GRIN2B | c.467T>A (p.Val156Glu) | |
12 | g.13753861C>A | CA384054751 | GRIN2B | c.466G>T (p.Val156Leu) | |
12 | g.13753861C= | CA2017525986 | GRIN2B | c.466G= (p.Val156=) | |
12 | g.13753861C>G | CA384054753 | GRIN2B | c.466G>C (p.Val156Leu) | |
12 | g.13753861C>T | CA384054755 | GRIN2B | c.466G>A (p.Val156Ile) | ClinVar dbSNP gnomAD v4 COSMIC |
12 | g.13753862G>A | CA6461397 | GRIN2B | c.465C>T (p.Ser155=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.13753862G>C | CA478853524 | GRIN2B | c.465C>G (p.Ser155=) | |
12 | g.13753862G= | CA2017525987 | GRIN2B | c.465C= (p.Ser155=) | |
12 | g.13753862G>T | CA225833 | GRIN2B | c.465C>A (p.Ser155=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.13753863G>A | CA384054759 | GRIN2B | c.464C>T (p.Ser155Phe) | |
12 | g.13753863G>C | CA384054760 | GRIN2B | c.464C>G (p.Ser155Cys) | |
12 | g.13753863G>T | CA384054762 | GRIN2B | c.464C>A (p.Ser155Tyr) | COSMIC |
12 | g.13753864A>C | CA384054765 | GRIN2B | c.463T>G (p.Ser155Ala) | |
12 | g.13753864A>G | CA384054767 | GRIN2B | c.463T>C (p.Ser155Pro) | |
12 | g.13753864A>T | CA384054763 | GRIN2B | c.463T>A (p.Ser155Thr) | |
12 | g.13753865A>C | CA478853526 | GRIN2B | c.462T>G (p.Ala154=) | |
12 | g.13753865A>G | CA478853527 | GRIN2B | c.462T>C (p.Ala154=) | |
12 | g.13753865A>T | CA478853528 | GRIN2B | c.462T>A (p.Ala154=) | |
12 | g.13753866G>A | CA384054768 | GRIN2B | c.461C>T (p.Ala154Val) | |
12 | g.13753866G>C | CA384054771 | GRIN2B | c.461C>G (p.Ala154Gly) | |
12 | g.13753866G>T | CA384054769 | GRIN2B | c.461C>A (p.Ala154Asp) | |
12 | g.13753867C>A | CA384054773 | GRIN2B | c.460G>T (p.Ala154Ser) | |
12 | g.13753867C= | CA2017525988 | GRIN2B | c.460G= (p.Ala154=) | |
12 | g.13753867C>G | CA384054775 | GRIN2B | c.460G>C (p.Ala154Pro) | |
12 | g.13753867C>T | CA384054776 | GRIN2B | c.460G>A (p.Ala154Thr) | dbSNP |
12 | g.13753868T>A | CA384054778 | GRIN2B | c.459A>T (p.Gln153His) | |
12 | g.13753868T>C | CA478853530 | GRIN2B | c.459A>G (p.Gln153=) | |
12 | g.13753868T>G | CA384054779 | GRIN2B | c.459A>C (p.Gln153His) | |
12 | g.13753869T>A | CA384054780 | GRIN2B | c.458A>T (p.Gln153Leu) | |
12 | g.13753869T>C | CA384054782 | GRIN2B | c.458A>G (p.Gln153Arg) | |
12 | g.13753869T>G | CA384054784 | GRIN2B | c.458A>C (p.Gln153Pro) | |
12 | g.13753870G>A | CA384054785 | GRIN2B | c.457C>T (p.Gln153Ter) | dbSNP |
12 | g.13753870G>C | CA384054786 | GRIN2B | c.457C>G (p.Gln153Glu) | |
12 | g.13753870G= | CA2017525989 | GRIN2B | c.457C= (p.Gln153=) | |
12 | g.13753870G>T | CA384054787 | GRIN2B | c.457C>A (p.Gln153Lys) | |
12 | g.13753871C>A | CA384054789 | GRIN2B | c.456G>T (p.Gln152His) | |
12 | g.13753871C= | CA2017525990 | GRIN2B | c.456G= (p.Gln152=) | |
12 | g.13753871C>G | CA384054788 | GRIN2B | c.456G>C (p.Gln152His) | |
12 | g.13753871C>T | CA6461398 | GRIN2B | c.456G>A (p.Gln152=) | dbSNP ExAC gnomAD v2 |
12 | g.13753872T>A | CA384054791 | GRIN2B | c.455A>T (p.Gln152Leu) | |
12 | g.13753872T>C | CA384054792 | GRIN2B | c.455A>G (p.Gln152Arg) | |
12 | g.13753872T>G | CA384054793 | GRIN2B | c.455A>C (p.Gln152Pro) | COSMIC |
12 | g.13753873G>A | CA384054795 | GRIN2B | c.454C>T (p.Gln152Ter) | dbSNP |
12 | g.13753873G>C | CA384054797 | GRIN2B | c.454C>G (p.Gln152Glu) | |
12 | g.13753873G= | CA2017525991 | GRIN2B | c.454C= (p.Gln152=) | |
12 | g.13753873G>T | CA384054798 | GRIN2B | c.454C>A (p.Gln152Lys) | |
12 | g.13753874T>A | CA384054800 | GRIN2B | c.453A>T (p.Glu151Asp) | |
12 | g.13753874T>C | CA478853533 | GRIN2B | c.453A>G (p.Glu151=) | dbSNP |
12 | g.13753874T>G | CA384054801 | GRIN2B | c.453A>C (p.Glu151Asp) | |
12 | g.13753874T= | CA2017525992 | GRIN2B | c.453A= (p.Glu151=) | |
12 | g.13753875T>A | CA384054803 | GRIN2B | c.452A>T (p.Glu151Val) | |
12 | g.13753875T>C | CA384054805 | GRIN2B | c.452A>G (p.Glu151Gly) | |
12 | g.13753875T>G | CA384054807 | GRIN2B | c.452A>C (p.Glu151Ala) | |
12 | g.13753876C>A | CA384054812 | GRIN2B | c.451G>T (p.Glu151Ter) | dbSNP gnomAD v4 |
12 | g.13753876C= | CA2017525993 | GRIN2B | c.451G= (p.Glu151=) | |
12 | g.13753876C>G | CA384054810 | GRIN2B | c.451G>C (p.Glu151Gln) | |
12 | g.13753876C>T | CA384054808 | GRIN2B | c.451G>A (p.Glu151Lys) |