ClinVar Miner

List of variants in gene NSD1 reported as likely benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 96
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HGVS dbSNP gnomAD frequency
NM_022455.5(NSD1):c.4967-175G>T rs80104688 0.02601
NM_022455.5(NSD1):c.1237-87dup rs149092444 0.02433
NM_022455.5(NSD1):c.3796+290del rs1562214821 0.01527
NM_022455.5(NSD1):c.5510-112G>A rs59258749 0.01246
NM_022455.5(NSD1):c.4302+252G>C rs115723131 0.00836
NM_022455.5(NSD1):c.4966+160A>G rs139502611 0.00827
NM_022455.5(NSD1):c.3796+21dup rs552714235 0.00822
NM_022455.5(NSD1):c.6152-171T>C rs79027751 0.00812
NM_022455.5(NSD1):c.5146+255T>C rs192689485 0.00701
NM_022455.5(NSD1):c.6259-59G>A rs76116584 0.00687
NM_022455.5(NSD1):c.4497+141A>G rs71601347 0.00669
NM_022455.5(NSD1):c.3797-66C>A rs114246039 0.00632
NM_022455.5(NSD1):c.6463+250C>A rs537540896 0.00621
NM_022455.5(NSD1):c.4302+133A>G rs114680977 0.00589
NM_022455.5(NSD1):c.6151+137G>A rs115143521 0.00513
NM_022455.5(NSD1):c.5510-286del rs201566409 0.00457
NM_022455.5(NSD1):c.-17-106A>G rs73806730 0.00454
NM_022455.5(NSD1):c.5304-190T>G rs73806745 0.00454
NM_022455.5(NSD1):c.3797-283T>C rs116559875 0.00452
NM_022455.5(NSD1):c.4497+329dup rs201565305 0.00452
NM_022455.5(NSD1):c.5146+84T>C rs141637983 0.00451
NM_022455.5(NSD1):c.-17-340C>T rs116419640 0.00450
NM_022455.5(NSD1):c.5147-49A>C rs74436451 0.00398
NM_022455.5(NSD1):c.6151+221A>G rs137945358 0.00349
NM_022455.5(NSD1):c.6009+201_6009+203dup rs558016724 0.00164
NM_022455.5(NSD1):c.3215G>A (p.Arg1072Gln) rs28932180 0.00036
NM_022455.5(NSD1):c.4497+52C>T rs372432409 0.00031
NM_022455.5(NSD1):c.2696T>C (p.Ile899Thr) rs142703625 0.00028
NM_022455.5(NSD1):c.3692G>A (p.Gly1231Glu) rs141065357 0.00020
NM_022455.5(NSD1):c.6991G>A (p.Asp2331Asn) rs772981865 0.00019
NM_022455.5(NSD1):c.2427G>A (p.Glu809=) rs61744224 0.00018
NM_022455.5(NSD1):c.7352G>A (p.Arg2451Lys) rs200115665 0.00018
NM_022455.5(NSD1):c.1558G>A (p.Ala520Thr) rs559617787 0.00017
NM_022455.5(NSD1):c.7576C>T (p.Pro2526Ser) rs373932824 0.00016
NM_022455.5(NSD1):c.5303+23A>G rs375503261 0.00012
NM_022455.5(NSD1):c.7933C>T (p.Leu2645=) rs61730553 0.00012
NM_022455.5(NSD1):c.1478C>T (p.Pro493Leu) rs140583358 0.00011
NM_022455.5(NSD1):c.4966+6G>A rs373129093 0.00010
NM_022455.5(NSD1):c.1477C>G (p.Pro493Ala) rs375051877 0.00009
NM_022455.5(NSD1):c.4187C>T (p.Thr1396Met) rs747298351 0.00009
NM_022455.5(NSD1):c.6429C>T (p.His2143=) rs121908068 0.00009
NM_022455.5(NSD1):c.2465C>G (p.Ser822Cys) rs377684553 0.00008
NM_022455.5(NSD1):c.1095C>T (p.Tyr365=) rs200080728 0.00007
NM_022455.5(NSD1):c.3089T>C (p.Leu1030Ser) rs200856103 0.00007
NM_022455.5(NSD1):c.3090G>T (p.Leu1030Phe) rs201860097 0.00007
NM_022455.5(NSD1):c.684A>G (p.Pro228=) rs1057522319 0.00006
NM_022455.5(NSD1):c.3741G>A (p.Met1247Ile) rs760307871 0.00005
NM_022455.5(NSD1):c.4303-4A>G rs775759198 0.00005
NM_022455.5(NSD1):c.7251A>T (p.Arg2417Ser) rs776952596 0.00005
NM_022455.5(NSD1):c.2350C>G (p.Gln784Glu) rs374740802 0.00004
NM_022455.5(NSD1):c.2425G>A (p.Glu809Lys) rs371421105 0.00004
NM_022455.5(NSD1):c.2766G>A (p.Thr922=) rs369705297 0.00004
NM_022455.5(NSD1):c.4307A>G (p.Tyr1436Cys) rs574641900 0.00004
NM_022455.5(NSD1):c.5007C>T (p.His1669=) rs146414176 0.00004
NM_022455.5(NSD1):c.7367T>C (p.Met2456Thr) rs761179792 0.00004
NM_022455.5(NSD1):c.1830A>G (p.Gln610=) rs759706066 0.00003
NM_022455.5(NSD1):c.3588G>T (p.Val1196=) rs549662786 0.00003
NM_022455.5(NSD1):c.5106T>C (p.His1702=) rs778450121 0.00003
NM_022455.5(NSD1):c.6788C>T (p.Ser2263Leu) rs373571733 0.00003
NM_022455.5(NSD1):c.682C>G (p.Pro228Ala) rs770522999 0.00003
NM_022455.5(NSD1):c.7500G>C (p.Met2500Ile) rs770120153 0.00003
NM_022455.5(NSD1):c.1495G>A (p.Ala499Thr) rs587784075 0.00002
NM_022455.5(NSD1):c.1763A>G (p.Asp588Gly) rs1046371505 0.00002
NM_022455.5(NSD1):c.198A>G (p.Pro66=) rs1057523994 0.00002
NM_022455.5(NSD1):c.7562C>A (p.Ala2521Asp) rs775806970 0.00002
NM_022455.5(NSD1):c.1894C>A (p.Arg632=) rs1481136060 0.00001
NM_022455.5(NSD1):c.2345G>A (p.Ser782Asn) rs769773081 0.00001
NM_022455.5(NSD1):c.293A>T (p.Gln98Leu) rs779850742 0.00001
NM_022455.5(NSD1):c.3056G>A (p.Arg1019His) rs750354456 0.00001
NM_022455.5(NSD1):c.34T>C (p.Cys12Arg) rs143406017 0.00001
NM_022455.5(NSD1):c.3512G>A (p.Arg1171His) rs111638717 0.00001
NM_022455.5(NSD1):c.6408A>G (p.Pro2136=) rs771993179 0.00001
NM_022455.5(NSD1):c.7631C>T (p.Ala2544Val) rs758398402 0.00001
NM_022455.5(NSD1):c.7780G>A (p.Ala2594Thr) rs146010779 0.00001
NM_022455.5(NSD1):c.8050G>A (p.Ala2684Thr) rs188326949 0.00001
NM_022455.5(NSD1):c.1064-10C>T rs1057523596
NM_022455.5(NSD1):c.1237-108C>A rs1407014054
NM_022455.5(NSD1):c.1237-92del rs560987364
NM_022455.5(NSD1):c.1596C>T (p.Asn532=) rs1554188977
NM_022455.5(NSD1):c.1852A>G (p.Lys618Glu)
NM_022455.5(NSD1):c.2655A>G (p.Ser885=) rs1437774200
NM_022455.5(NSD1):c.3171T>C (p.Asn1057=) rs1763344554
NM_022455.5(NSD1):c.3796+282_3796+295del rs758221753
NM_022455.5(NSD1):c.4302+341_4302+342del rs142778014
NM_022455.5(NSD1):c.4765+10A>T rs1554198444
NM_022455.5(NSD1):c.4966+76_4966+77insTTTT rs1343529552
NM_022455.5(NSD1):c.4966+93_4966+96dup rs373383515
NM_022455.5(NSD1):c.4966+96dup rs373383515
NM_022455.5(NSD1):c.507C>T (p.Asp169=) rs201012228
NM_022455.5(NSD1):c.5303+35A>C rs372649300
NM_022455.5(NSD1):c.6151+287A>G rs115142140
NM_022455.5(NSD1):c.7115C>A (p.Pro2372His) rs1057522686
NM_022455.5(NSD1):c.7144A>G (p.Thr2382Ala) rs765876148
NM_022455.5(NSD1):c.750AGC[1] (p.Ala252del) rs398124385
NM_022455.5(NSD1):c.7809C>T (p.Leu2603=) rs769301382
NM_022455.5(NSD1):c.91C>G (p.Pro31Ala) rs905320202

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